- Biopsy, Bone Marrow, Trephine and Clot
- Biopsy, Extra (5 or More Blocks)
- Biopsy, Multiple (2 to 4 Blocks)
- Biopsy, Simple
- Biopsy, Special, Intestine for Hirschsprung Disease
- Biopsy, Special, Liver
- Biopsy, Special, Metabolic Bone
- Biopsy, Special, Miscellaneous
- Biopsy, Special, Nerve
- Biopsy, Special, Renal
- Biopsy, Special, Skeletal Muscle
- Biopsy, Special, Skin
- Biopsy, Special, Skin, with Immunofluorscent Study
- Biopsy, Special, Tissue for Lymphoma Study
- Biopsy, Special, Transplant
- Frozen Section with Intraoperative Consultation
- Frozen Section, per Case
- Frozen Specimen Processing, Miscellaneous
- Gross Examination Only
- Histopathological Examination, per Case
- Perimortem Specimen
- Surgical Specimen, High Complexity
- Surgical Specimen, Low Complexity
- Surgical Specimen, Moderate Complexity
- Surgical Specimen, Simple
- Surgical Specimen, Wire-guided
- Surgical Specimen, with Special Examination
- Crystal Identification, Fluid (Microscopy)
- Cytology, Bronchial, for Pnuemocystis carinii
- Cytology, for Eosinophils
- Cytology, for Haemosiderin
- Cytology, for Lipid-laden Macrophages
- Cytology, for Sex Chromatin Identification [Barr Bodies]
- Cytology, GYN (Conventional Pap Smear)
- Cytology, GYN (Conventional Pap Smear), with Interpretation by Pathologist
- Cytology, GYN (Liquid-Based)
- Cytology, GYN (Liquid-Based) + Human Papillomavirus [HPV] Detection (Digene Test) (Profile)
- Cytology, GYN (Liquid-Based), with Interpretation by Pathologist
- Cytology, GYN, with Special Examination
- Cytology, GYN, with Special Examination (Profile)
- Cytology, Non-GYN
- Cytology, Non-GYN (Liquid-based)
- Cytology, Non-GYN (Liquid-based), with Interpretation by Pathologist
- Cytology, Non-GYN, Bronchial
- Cytology, Non-GYN, CSF
- Cytology, Non-GYN, Miscellaneous
- Cytology, Non-GYN, Peritoneal
- Cytology, Non-GYN, Pleural
- Cytology, Non-GYN, Sputum
- Cytology, Non-GYN, Urine
- Cytology, Non-GYN, with Interpretation by Pathologist
- Cytology, Non-GYN, with Special Examination
- Cytology, Sputum, for Pnuemocystis carinii
- Exfoliative Cytology, per Case
- Fine Needle Aspiration Cytology, per Case
- Fine Needle Aspiration, Imaging-guided, Specimen Only
- Fine Needle Aspiration, Imaging-guided, with Procedure Attendence
- Fine Needle Aspiration, Specimen Only
- Fine Needle Aspiration, with Clinical Consultation
- Miscellaneous Body Fluid Microcopy
- Vaginal Smear for Hormonal Status
- Autopsy, Clinical
- Autopsy, Clinical, Limited
- Autopsy, Perinatal
- Post-mortem Examination, Including Microscopic Study
- Case Review or Consultation, Autopsy
- Case Review or Consultation, Cytology
- Case Review or Consultation, Histopathlogy
- Case Review or Consultation, with Special Procedures
- Electron Microscopy Procedure - Scan and Photography
- Electron Microscopy Procedure - Semithin Section
- Electron Microscopy Procedure - Tissue Processing
- Electron Microscopy Procedure - Ultrathin Section
- Electron Microscopy, Complete, with Interpretation
- EM semi-thin section
- IHC MMR Assay
- Immunofluorescent Study Procedure
- Immunofluorescent Study with Interpretation
- Immunohistochemistry Procedure
- Immunohistochemistry with Interpretation
- Miscellaneous Special Laboratory Procedure
- Miscellaneous Special Laboratory Procedure with Interpretation
- Scanning Electron Microscopy Procedure
- Scanning Electron Microscopy with Interpretation
- (1,3)-Beta-D-Glucan, Serum
- Actinomyces Culture
- Aerobic Plate Count
- Albumin & Glucose, Urine
- Amikacin - Peak Level
- Amikacin - Random Level
- Amikacin - Trough Level
- Amphotericin B - Peak Level
- Amphotericin B - Random Level
- Amphotericin B - Trough Level
- Anaerobic Culture
- Antibiotic Level, Serum
- Antibiotic Sensitivity Test
- Atypical Mycobacterial Culture
- Bacterial Culture & Microscopy
- Bacterial Culture & Microscopy, CSF
- Bacterial Culture & Microscopy, Stool
- Bacterial Culture & Microscopy, Urine
- Bacterial Culture with Sensitivity Test
- Bacterial Culture, All Types of Specimen (No Sensitivity Test Result)
- Bacterial Culture, Body Fluid
- Bacterial Culture, CAPD Fluid
- Bacterial Culture, CSF
- Bacterial Culture, Donor Blood/Blood Product
- Bacterial Culture, Genital Tract Specimen
- Bacterial Culture, Respiratory Specimen
- Bacterial Culture, Sputum
- Bacterial Culture, Stool
- Bacterial Culture, Tissue
- Bacterial Culture, Urine
- Blood Culture
- Bordetella pertussis Culture
- Brucella Culture
- Cell Count and Microscopy, Body Fluid
- Cell Count, CSF
- Cell Count, Fluid
- Cell Count, Stool
- Clostridium difficile Antigen (GDH)
- Clostridium difficile Culture
- Corynebacterium diphtheriae Culture
- Cryptococcal Culture
- Cryptococcal Culture & Negative Stain
- Crystal Identification, Urine (Microscopy)
- Darkground Microscopy
- Dematophyte Culture
- Dermatophyte (Microscopy)
- Diphtheria Culture
- Dysmorphic Red Cells, Urine
- Endotoxin Testing, Dialysis Water
- Enterohaemorrhagic Escherichia coli Culture
- Escherichia coli O157 Culture
- Examination for Trichomoniasis
- Extended Spectrum Beta-Lactamases [ESBL] Producting Organism Screening
- Fluconazole - Peak Level
- Fluconazole - Random Level
- Fluconazole - Trough Level
- Food Poisoning Culture
- Fungal Culture
- Fungal Culture, Air Sampling
- Fungal Culture, All Types of Specimen
- Fungal Culture, Blood
- Fungal Microscopy & Culture
- Genatmicin - Peak Level
- Genatmicin - Random Level
- Genatmicin - Trough Level
- Gonococcal Culture
- Gram Smear for Microorganisms, All Types of Specimen (Microscopy)
- Gram Stain
- Group B Streptococcus Culture
- Haemophilus ducreyi Culture
- Helicobacater pylori Culture
- Legionella Antigen
- Legionella Culture
- Leptospira Culture
- Methicillin-resistant Staphylococcus aureus [MRSA] Screening
- Microscopy, Sputum
- Microscopy, Stool
- Microscopy, Urine
- Minimum Bactericidal Concentration [MBC]
- Minimum Inhibitory Concentration [MIC]
- Miscellaneous Culture with Sensitivity Test
- Miscellaneous Culture, no sensitivity test
- Multidrug-resistant Pseudomonas aeruginosa [MRPA] Screening
- Mycobacterial [Acid-Fast Bacilli] Culture & Sensitivity Test
- Mycobacterial [Acid-Fast Bacilli] Culture & Sensitivity Test and Smear
- Mycobacterial [Acid-Fast Bacilli] Culture (No Sensitivity Test Result)
- Mycobacterial [Acid-Fast Bacilli] Smear Only
- Mycobacterial Antibiotic Sensitivity Test
- Mycoplasma Culture
- Negative Stain
- Netilmicin - Peak Level
- Netilmicin - Random Level
- Netilmicin - Trough Level
- Nocardia Culture
- Routine & Microscopy, Urine
- Routine Examination, Urine
- Serum Bactericidal Titre
- Spore Strip Culture
- Sterility Culture
- Sterility Culture, Air Sampling
- Sterility Culture, Biological Products
- Sterility Culture, Environmental Sample
- Sterility Culture, Milk
- Sterility Culture, Nuclear Medicine Products
- Sterility Culture, Pharmaceutical Products
- Sterility Culture, R.O. Water
- Sterility Culture, Settle Plate
- Sterility Culture, Total Parental Nutrition [TPN]
- Sterility Test of Biological Products
- Streptococcus pneumoniae Antigen
- Surveillance Culture
- Tobramycin - Peak Level
- Tobramycin - Trough Level
- Tobramycin, Random Level
- Total Bacterial Count, environmental sample
- Trichomonas and Yeasts Examination
- Tuberculostearic Acid Assay
- Vancomycin - Peak Level
- Vancomycin - Random Level
- Vancomycin - Trough Level
- Vancomycin-resistant Enterococcus [VRE] Screening
- Vibrio cholerae Culture
- Yersinia Culture
- Adenosine Deaminase Test
- Amoeba Antibody
- Anti-Streptolysin-O Test [ASOT]
- Aspergillus Antigen
- Aspergillus fumigatus Antibody
- Bacterial Antigen (Latex Agglutination Test)
- Bacterial Antigen Test
- Blastomyces dermatitidis Antibody
- Borrelia burgdorferi Antibody
- Brucella Antibody
- Candida Antibody
- Clostridium difficile Toxin Assay (Cell Culture Method)
- Clostridium difficile Toxin Assay (EIA)
- Coccidioides immitis Antibody
- Cryptococcal Antigen
- Dimorphic Fungi Antibody
- Diphtheria Antibody
- Fungus Antibody
- Galactomannan Antigen
- Group B Streptococcus Latex Agglutination Test
- Helicobacter pylori Antibody - IgG
- Hepatitis B Surface Antigen(EIA)+Hepatitis B Core Antibody, Total+Hepatitis C Virus Surface Antibody[HCsAb](Automated)+Human Immunodeficiency Virus [HIV] Type 1 and 2 Antibodies(MEIA)
- Histoplasma capsulatum Antibody
- Legionella pneumophila Antibody
- Leptospira Antibody
- Leptospira Antibody - IgM
- Penicillium marneffei Antibody
- SARS-CoV-2 Antibody
- Shiga-like Toxin
- Tetanus Antibody
- Treponema pallidum (RPR)
- Treponema pallidum (VDRL)
- Treponema pallidum Antibody (EIA)
- Treponema pallidum Antibody (FTA-ABS)
- Treponema pallidum Antibody (FTA-ABS) - IgM
- Treponema pallidum Antibody (FTA-ABS) & Treponema pallidum (VDRL)
- Treponema pallidum Antibody (FTA-ABS) & Treponema pallidum (VDRL)
- Treponema pallidum Antibody (TPPA)
- Weil-Felix Test
- Widal Test
- Acanthamoeba Culture
- Amoeba Culture
- Amoeba Examination
- Cryptosporidium Examination
- Cyclospora Examination
- Cysticercosis Antibody
- Giardia Examination
- Isospora (Special Stain)
- Isospora Examination
- Leishmania Examination
- Microsporidium Examination
- Ova and Cyst Examination
- Parasite Identification
- Parasitic Infection Serology
- Parasitic Infections (Serology Test), per Species of Parasite
- Scabies Examination
- Toxoplasma gondii Antibody
- Toxoplasma gondii Antibody - IgA
- Toxoplasma gondii Antibody - IgG
- Toxoplasma gondii Antibody - IgM
- Trichinella Antibody
- Trophozoites Examination
- Worm Identification
- 1,25-dihydroxyvitamin D, serum
- 17-Alpha Hydroxyprogesterone
- 17-Alpha Hydroxyprogesterone, Maternal
- 17α-Hydroxyprogesterone(MS)
- Acetoacetate
- Acetone
- Acid Maltase
- Acid Phosphatase
- Acylcarnitine Profile
- Adrenaline
- Adrenocorticotropic Hormone [ACTH]
- Adrenocorticotropic Hormone [ACTH] & Cortisol [CORT]
- Adrenocorticotropic Hormone [ACTH] + Cortisol [CORT]
- Adrenocorticotropic Hormone [ACTH] + Cortisol [CORT] +17-Alpha Hydroxyprogesterone
- Adrenocorticotropic Hormone [ACTH], Inferior Petrosal Sinus Sampling
- Alanine Aminotransferase [ALT / SGPT]
- Albumin [ALB]
- Albumin [ALB] + Protein - Total
- Alcohol Profile (GC)
- Aldosterone
- Aldosterone + Renin (x 2)
- Aldosterone, Cortisol, Renin
- Aldosterone, Erect
- Aldosterone, Fluid
- Aldosterone, Supine
- Alkaline Phosphatase - Bone-specific
- Alkaline Phosphatase (Electrophoresis)
- Alkaline Phosphatase (Heat Stability Test)
- Alkaline Phosphatase [ALP]
- Alpha & Beta Galactosidase
- Alpha-1-Antitrypsin
- Alpha-Fetoprotein
- Alpha-Fetoprotein - Maternal
- Alpha-Subunit of Glycoprotein Hormones
- Aluminium
- Amino Acid - 1-Methyl Histidine
- Amino Acid - Alanine
- Amino Acid - Allo-Isoleucine
- Amino Acid - Alpha Aminobutyric Acid
- Amino Acid - Arginine
- Amino Acid - Asparagine
- Amino Acid - Aspartic Acid
- Amino Acid - Beta Alanine
- Amino Acid - Citrulline
- Amino Acid - Cystine
- Amino Acid - Gamma Aminobutyric Acid
- Amino Acid - Glutamic Acid
- Amino Acid - Glutamine
- Amino Acid - Histidine
- Amino Acid - Homocysteine (HPLC)
- Amino Acid - Homocysteine, Total
- Amino Acid - Hydroxyproline
- Amino Acid - Isoleucine
- Amino Acid - Leucine
- Amino Acid - Methionine
- Amino Acid - Ornithine
- Amino Acid - Phenylalanine
- Amino Acid - Serine
- Amino Acid - Taurine
- Amino Acid - Threonine
- Amino Acid - Tryptophan
- Amino Acid - Tyrosine
- Amino Acid - Valine
- Amino Acid Chromatography with Quantitation
- Amino Acid Chromatography with Quantitation, including PKU Screening
- Ammonia
- Amylase
- Androstenedione
- Anticonvulsant Profile
- Antimony, Serum
- Anti-Mullerian Hormone
- Apo A1, Apo B and Lipid Profile
- Apolipoprotein A1 [Apo A1]
- Apolipoprotein A1 [Apo A1] + Apolipoprotein B [Apo B]
- Apolipoprotein B [Apo B]
- Apolipoprotein E [Apo E]
- Asparaginase
- Asparate Aminotransferase [AST / SGOT]
- Asparate Aminotransferase [AST / SGOT] + Creatine Kinase [CK]
- Barbiturate
- Beryllium, Serum
- Beta-Hydroxybutyrate
- Bicarbonate
- Bicarbonate + Chloride + Potassium + Sodium
- Bile Acid
- Bilirubin - Direct
- Bilirubin - Direct + Total
- Bilirubin - Neonatal
- Bilirubin - Total
- Bilirubin Delta
- Bilirubin, Conjugated
- Bilirubin, Subfractions [BuBc]
- Bilirubin, Unconjugated
- Blood Gas
- Blood Gas - Base Excess, In-vitro
- Blood Gas - Deoxyhaemoglobin
- Blood Gas - O2 Saturation
- Blood Gas - Oxyhaemoglobin
- Blood Gas - pCO2
- Blood Gas - pH
- Blood Gas - pO2
- Blood Gas & Na, K, iCa (Capillary)
- Blood Gas & Na/K
- Blood Gas, Na/K, & iCa
- Bone Profile - ALP, Ca, Phos, ALB
- Bone Profile - Ca & Phosphate
- CA 19.9
- CA125
- Cadmium
- Caffeine
- Calcitonin
- Calcium
- Calcium - Albumin Adjusted
- Calcium - Ionised [iCa]
- Calcium [Ca]
- Calcium, Whole Blood
- Carbamazepine [Tegretol]
- Carboxyhaemoglobin
- Carcinoembyonic Antigen [CEA]
- Cardiac Enzymes - CK, LDH, AST
- Cardiac Enzymes with CK-MB Activity - AST, CK, CK-MB
- Cardiac Enzymes with CK-MB Activity - AST, CK, CK-MB + Renal Function Test
- Cardiac Enzymes with CK-MB Activity - AST, CK, CK-MB + Troponin I
- Cardiac Enzymes with CK-MB Activity - AST, CK, CK-MB + Troponin I + Liver Function Tests [LFT] - Total Protein, Albumin, Total Bilirubin, Alkali
- Cardiac Enzymes with CK-MB Activity - AST, CK, CK-MB + Troponin I + Renal Function Tests [RFT] - Creatinine, Potassium, Sodium and Urea
- Carnitine - Free
- Carnitine - Free & Total
- Carnitine - Total
- Carotenoids
- Catecholamines
- Cerulopasmin
- Chloride
- Chloride, Whole Blood
- Cholesterol
- Cholesterol - HDL
- Cholesterol - LDL (Direct Measurement)
- Cholesterol - Low Density Lipid [LDL] (Direct Measurement)
- Cholesterol - VLDL (Calculated)
- Cholesterol & Triglycerides
- Chromium, Serum
- Clobazam, serum
- Clonazepam [Rivotril]
- Cobalt, Serum
- Copper
- Cortisol - Adrenal Venous Sampling
- Cortisol - Adrenal Venous Sampling & Aldosterone
- Cortisol [CORT]
- Cortisol, AM
- Cortisol, PM
- C-Peptide
- C-Reactive Protein [CRP]
- Creatine
- Creatine Kinase [CK]
- Creatine Kinase [CK] & Lactate Dehydrogenase [LD]
- Creatine Kinase-MB [CK-MB]
- Creatine Kinase-MB [CK-MB] + Troponin I
- Creatine metabolism in plasma
- Creatinine
- Creatinine & Urea
- Cryoglobulins
- C-telopeptide of type I collagen (CTX)
- Cyanide
- Cyclosporin A
- Cyclosporin A - Peak
- Cyclosporin A - Timed
- Cyclosporin A - Trough
- Cyclosporin A - Trough or Timed
- Cystatin C, plasma
- Dehydroepaindrosterone Sulphate [DHEAS]
- Delta ALA Dehydratase [ALAD]
- Diazepam [Valium]
- Digoxin
- D-Lactate
- Dormicum [Midazolam]
- Dried blood spot Acid-alpha glucosidase activity test
- Dried blood spot Acid-beta-glucocerebrosidase activity test
- Dried blood spot Acid-sphingomyelinase activity test
- Dried blood spot Alpha-galactosidase A activity test
- Dried blood spot Alpha-L-iduronidase activity test
- Dried blood spot Beta galactocerebrosidase activity test
- Dried Blood Spot for 17OHP activity
- Dried Blood Spot for Biotinidase activity
- Dried Blood Spot for GALT activity
- Estradiol [E2]
- Ethanol
- Ethosuximide [Zarontin]
- Everolimus
- Fatty Acids, Very Long Chain
- Ferritin
- Fibroblast growth factor 21
- Flecainide, serum
- Folate, Red Cell
- Folate, Serum
- Follicule Stimulating Hormone [FSH]
- Follicule Stimulating Hormone [FSH] + Luteinizing Hormone [LH] + Estradiol [E2]
- Follicule Stimulating Hormone [FSH] + Luteinizing Hormone [LH] + Estradiol [E2] + 17-Alpha Hydroxyprogesterone + Testosterone
- Free Fatty Acids
- Fructosamine [FRUC]
- Gabapentin
- Galactose -1-Phosphate Uridyl Transferase [GPUT]
- Gamma Glutamyl Transferase - Paediatric
- Gamma Glutamyl Transferase [GGT]
- Gastrin
- Globulin
- Glomerular Filtration Rate [GFR]
- Glucose [GLU]
- Glucose [GLU] + Growth Hormone [GH]
- Glucose [GLU] + Insulin
- Glucose [GLU] + Insulin + C-Peptide
- Glucose [GLU] + Insulin + C-Peptide + Growth Hormone + Cortisol [CORT]
- Glucose + Growth Hormone [GH] + Cortisol + Luteinizing Hormone [LH] + Dynamic Test - Thyroid Stimulating Hormone [TSH] Test + Prolactin
- Glucose 6-Phosphate Dehydrogenase [G6PD]
- Glucose 6-Phosphate Dehydrogenase [G6PD] - Quantitative
- Glucose Tolerance Test
- Glucose, 2 Hr Postprandial
- Glucose, Fasting
- Glucose, Whole Blood
- Glucose-6-phosphate dehydrogenase, quantitative
- Growth Hormone [GH]
- Growth Hormone [GH] + Cortisol [CORT] + Adrenocorticotropic Hormone [ACTH] + Glucose [GLU]
- Growth Hormone [GH] + Insulin-like Growth Factor 1 [IGF1]
- Haptoglobin
- Hexosaminidase A & B
- Homocysteine (HPLC)
- Homocysteine, Total
- Human Chorionic Gonadotrophin [HCG]
- Human Chorionic Gonadotrophin [HCG], Semi-Quantitative
- Immunoglobulin D level
- Immunoglobulin G Subclasses Profile
- Immunoglobulin G, A & M
- Immunoglobulin G4 Subclass
- Immunoglobulin M level, serum
- Insulin
- Insulin + Glucose + Growth Hormone + Insulin-like Growth Factor 1 [IGF1]
- Insulin-like Growth Factor
- Insulin-like Growth Factor 1 [IGF1]
- Insulin-Like Growth Factor Binding Protein 3
- Iodine, Serum
- Iron
- Iron & Iron Binding Capacity, Total [TIBC]
- Iron & Iron Binding Capacity, Total [TIBC] & Ferritin
- Iron Binding Capacity, Total [TIBC]
- Iron Profile
- Isopropanol
- Ketone Bodies, Qualitative
- Ketone Profile - Free Fatty Acids, B-Hydroxybutyrate & Acetoacetate
- Lactate Dehydrogenase [LD]
- Lactate Pyruvate Meal Challenge Test
- Lactic Acid [Lactate]
- Lactic Acid, Whole Blood
- Lamotrigine [Lamictal]
- Lead
- Lipase
- Lipid Fraction (Ultracentrifugation)
- Lipid Profile - Cholesterol & Triglyceride
- Lipid Profile - Cholesterol, Triglyceride, LDL (Calculated), HDL
- Lipid Profile - Cholesterol, Triglyceride, LDL (Calculated), HDL + Renal and Liver Function Tests+ Urate
- Lipoprotein Pattern
- Lipoprotein(a) [Lp(a)]
- Lithium
- Liver Function Tests [LFT] - Total Protein, Albumin, Total Bilirubin, Alkaline Phosphatase, Alanine Aminotransferase
- Liver Function Tests [LFT] - Total Protein, Albumin, Total Bilirubin, Alkaline Phosphatase, Alanine Aminotransferase + Amylase
- Liver Function Tests [LFT] - Total Protein, Albumin, Total Bilirubin, Alkaline Phosphatase, Alanine Aminotransferase + Cardiac Enzymes - CK, LDH, AST
- Liver Function Tests [LFT] - Total Protein, Albumin, Total Bilirubin, Alkaline Phosphatase, Alanine Aminotransferase + Gamma Glutamyl Transferase [GGT]
- Liver Function Tests, Neonatal - Total Protein, Albumin, Bilirubin Subfractions, Alkaline Phosphatase, Alanine Aminotransferase, Gamma-Glutamyl Transferase
- Liver Function Tests, Paediatric - Total Protein, Albumin, Total Bilirubin, Alkaline Phosphatase, Alanine Aminotransferase, Gamma-Glutamyl Transferase
- Lorazepam [Ativan]
- Luteinizing Hormone [LH]
- Lysozyme
- Magnesium
- Manganese [Mn]
- MDRD - Estimated GFR [eGFR] using Modification of Diet in Renal Disease Formula
- Mercury, Whole Blood
- Metabolic Screen, Blood (Dried Blood Spot)
- Metabolic Screen, Blood (GCMS)
- Methaemoglobin [MetHb]
- Methanol, Qualitative
- Methanol, Quantitative
- Methotrexate
- Methylmalonic Acid
- Mycophenolic acid
- Nickel, Serum
- Nitrazepam [Mogadon]
- Noradrenaline
- Nordiazepam
- NT-pro BNP (N-terminal pro B-type natriuretic peptide)
- Osmolality
- Overnight Dexamethasone Test
- Oxyhaemoglobin
- Paracetamol
- Paraprotein (Immunofixation)
- Parathyroid Hormone - Intraoperative
- Parathyroid Hormone - Selective Venous Sampling
- Parathyroid Hormone [PTH]
- Parathyroid Hormone [PTH] with Calcium
- Phenobarbital [Luminal]
- Phenytoin [Dilantin]
- Phosphate - Inorganic [Phos]
- Phytosterols
- Pigments (Spectroscopy)
- Plasma Metanephrines
- Posaconazole
- Potassium & Sodium - Paediatric
- Potassium [K]
- Potassium [K] + Blood Gas - pH
- Potassium, Whole Blood
- Prealbumin [PAB]
- Procollagen type I N-terminal propeptide (P1NP)
- Progesterone
- Prolactin [PRL]
- Propafenone, serum
- Prostate Health Index (Profile)
- Prostate Specific Antigen
- Protein - Total
- Protein - Total + Albumin [ALB] + Globulin
- Protein Electrophoresis
- Pseudocholinesterase
- Pseudo-Cholinesterase - with Fluoride and Dibucaine Numbers
- Pyruvate
- Renal and Liver Function Tests
- Renal and Liver Function Tests + Amylase
- Renal and Liver Function Tests + Bone Profile - Ca & Phos
- Renal and Liver Function Tests + Bone Profile - Ca & Phos + Creatine Kinase [CK] + Lactate Dehydrogenase [LD]
- Renal and Liver Function Tests + Bone Profile - Ca & Phos + Creatine Kinase [CK] + Lactate Dehydrogenase [LD] + Glucose
- Renal and Liver Function Tests + Bone Profile - Ca & Phos + Glucose
- Renal and Liver Function Tests + Bone Profile - Ca + Phosphate& Cardiac Enzymes - CK, LDH, AST
- Renal and Liver Function Tests + Cardiac Enzymes - CK, LDH, AST
- Renal and Liver Function Tests + Cardiac Enzymes with CK-MB Activity - AST, CK, CK-MB + Troponin I
- Renal and Liver Function Tests + Gamma Glutamyl Transferase [GGT]
- Renal and Liver Function Tests + Hepatitis B Surface Antigen (EIA)
- Renal and Liver Function Tests, Paediatric
- Renal Function Tests [RFT] - Creatinine, Potassium, Sodium and Urea
- Renal Function Tests [RFT] - Creatinine, Potassium, Sodium and Urea + Amylase
- Renal Function Tests [RFT] - Creatinine, Potassium, Sodium and Urea + Cardiac Enzymes - CK, LDH, AST
- Renal Function Tests [RFT] - Creatinine, Potassium, Sodium and Urea + Gamma Glutamyl Transferase [GGT]
- Renal Function Tests, Paediatric
- Renin
- Renin, Erect
- Renin, Suprine
- Salicylates [Aspirin]
- Selenium, Serum
- Serum chromogranin A
- Serum Vitamin D
- Sex Hormone Binding Globulin [SHBG]
- Sirolimus
- Sodium [Na]
- Sodium [Na] + Potassium [K]
- Sodium [Na] + Potassium [K] + Urea
- Sodium [Na] + Potassium [K] + Urea + Calcium [Ca]
- Tacrolimus - Peak
- Tacrolimus - Timed
- Tacrolimus - Trough
- Tacrolimus [FK506]
- Testosterone
- Testosterone (MS)
- Testosterone + Albumin [ALB] + Sex Hormone Binding Globulin [SHBG]
- Testosterone, Maternal
- Thallium, Serum
- Theophylline [Aminophylline]
- Thiopentone
- Thyroglobulin & Thyroglobulin Antibodies, Quantitative
- Thyroglobulin, Qualitative
- Thyroid stimulating hormone
- Thyroid Stimulating Hormone [TSH]
- Thyroid Stimulating Hormone [TSH] + Thyroxine [T4] - Free
- Thyroid Stimulating Hormone [TSH] + Thyroxine [T4] - Free + Thyroxine [T4] - Total
- Thyroid Stimulating Hormone [TSH] + Thyroxine [T4] - Free + Triiodothyronine [T3] - Free + Alpha-Subunit of Glycoprotein Hormones + Prolactin [PRL]
- Thyroxine [T4] - Free
- Thyroxine [T4] - Free / Triiodothyronine [T3] - Free
- Thyroxine [T4] - Total
- Thyroxine, free (FT4)
- Transferrin [TRF]
- Transketolase, Erythrocyte with TPP
- Triglycerides
- Triglycerides + Cholesterol + Cholesterol - HDL
- Triiodothyronine [T3] - Free
- Triiodothyronine [T3] - Total
- Troponin I
- Troponin T
- Urea
- Urea & Creatinine
- Uric Acid [Urate]
- Valproic Acid [Epilim]
- Vanadium, Serum
- Vigabatrin [Sabril]
- Vitamin A
- Vitamin B1
- Vitamin B12
- Vitamin B12 & Folate
- Vitamin B2
- Vitamin B6
- Vitamin D [25-OH]
- Vitamin E
- Whole Blod Bilirubin
- Xylose
- Zinc, RBC
- Zinc, Serum
- Busulfan TDM Profile
- Clomiphene Stimulation Test [CLST] - {E2 x 0' + FSH x 0', 30', 60'}
- Clomiphene Stimulation Test [CLST] - {E2 x 0' + FSH, LH x 0', 30', 60'}
- Clomiphene Stimulation Test [CLST] - {E2 x 0' + LH x 0', 30', 60'}
- Clomiphene Stimulation Test [CLST] - {FSH, LH x 0', 30', 60'}
- Clonidine Stimulation Test [GLST2] - {CORT, GH x 0', 30', 60', 90', 120'}
- Clonidine Stimulation Test [GLST2] - {GH x 0', 30', 60', 90', 120', 150', 180'}
- Clonidine Stimulation Test [GLST2] - {GH x 0', 30', 60', 90', 120', 150'}
- Clonidine Stimulation Test [GLST2] - {IGF1 x 0' + GH x 0', 30', 60', 90', 120', 150', 180'}
- Clonidine Suppression Test - {Urine catecholamines - Adrenaline, Noradrenaline}
- Combined Synacthen Test - {CORT x 0', 30', 60', 240', 300'}
- Corticotropin Releasing Function Test [CRF] - {ACTH, CORT x 0', 15', 30', 60', 120'}
- Corticotropin Releasing Function Test [CRF] - {ACTH, CORT x 0', 5', 15', 30', 45', 60', 90'}
- Corticotropin Releasing Function Test [CRF] - {ACTH, CORT x -15', 0', 15' 30' 45' 60' 90' 120'}
- Corticotropin Releasing Function Test [CRF] - {ACTH, CORT x -15', 0', 15', 30', 60', 90', 120'}
- Desmopressin Test - {ACTH, CORT x -15', 0', 15', 30', 45', 60', 90', 120'}
- Dexamethasone Suppression Test, High Dose - {CORT x Single Time Point}
- Dexamethasone Suppression Test, Low Dose - {CORT, ACTH x Single Time Point}
- Dexamethasone Suppression Test, Overnight - {CORT x Single Time Point}
- Domperidone Stimulation Test
- Dynamic Test - Low Dose Short Synacthen Test [LDSSYN] - {CORT x 0', 30'}
- Dynamic Test - Short Synacthen Test [LDSSYN] - {CORT x 0', 30'}
- Dynamic Test - Synacthen Test [LDSSYN] - {CORT x 0', 30'}
- Forearm Ischaemic Exercise Test - {Ammonia, Lactate, CK x 0', 1', 2', 5', 7', 10', 15'}
- Glucagon Stimulation Test [GCGT] - {CORT, GH, GLU x 0', 30', 60', 90', 120'}
- Glucagon Stimulation Test [GCGT] - {CORT, GH, GLU x 0', 60', 90', 120', 150', 180', 210'}
- Glucagon Stimulation Test [GCGT] - {CORT, GH, GLU x 0', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {CORT, GH, GLU x 0', 90', 120', 150', 180', 210', 240'}
- Glucagon Stimulation Test [GCGT] - {CORT, GH, GLU x -15', 0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {CORT, GH, GLU, INSU x -15' ,0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {CORT, GH, GLU, PRL x -15', 0', 30', 60', 90', 120', 150', 180', 210', 240'}
- Glucagon Stimulation Test [GCGT] - {CORT, GLU x 0', 60', 90', 120', 150', 180', 210'}
- Glucagon Stimulation Test [GCGT] - {C-PEP ,GH, CORT, GLU x -15' ,0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {C-PEP, CORT, GLU x -15', 0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {C-PEP, GH, GLU x -15', 0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {C-PEP, GLU x 0', 6'}
- Glucagon Stimulation Test [GCGT] - {C-PEP, GLU x -15' ,0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {C-PEP, INSU, CORT, GLU x -15', 0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {C-PEP, INSU, GH, CORT, GLU x -15', 0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {C-PEP, INSU, GH, GLU x -15', 0', 30', 60', 90', 120', 150', 180'}
- Glucagon Stimulation Test [GCGT] - {C-PEP, INSU, GLU x -15' ,0', 30', 60', 90', 120', 150', 180' }
- Glucagon Stimulation Test [GCGT] - {GH, GLU x 0', 30', 60', 90', 120'}
- Glucagon Stimulation Test [GCGT] - {GH, GLU, INSU x -15' ,0' , 30', 60', 90', 120', 150', 180'}
- Glucose Profile - {GLU x 0', 120', 240', 480'}
- Glucose Profile - {GLU x 0', 5', 10', 15', 20', 25', 30'}
- Glucose Profile - {GLU x -10', -5', 0', 15', 30', 60', 120'}
- Glucose Suppression test [EGTT] - {GH, GLU x 0', 30', 60', 90', 120'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU x 0', 120', 180'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU x 0', 120'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU x 0', 30', 60', 90', 120' 150' + GH x 0', 90', 150'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU x 0', 30', 60', 90', 120', 180', 240', 300'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU x 0', 60', 120', 180'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU x 0', 60', 120'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU x 0', 60'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, GH x 0', 30', 60', 120', 180'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, GH x 0', 30', 60', 90', 120', 150', 180'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, GH x 0', 30', 60', 90', 120', 150'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, GH x 0', 30', 60', 90', 120', 180'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, GH x 0', 60', 120'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, GH x 0', 90', 150'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, GH, INSU x 0', 30', 60'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, INSU x 0', 120'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, INSU x 0', 30' 120' 150, 180'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, INSU x 0', 30' 120'}
- Glucose Tolerance Test, Oral [OGTT] - {GLU, INSU x 0', 30', 60', 90', 120', 150'}
- Glucose Tolerance Test, Oral [OGTT] - {IGF1 x 0' + GH, GLU x 0', 30', 60', 90', 120', 150'}
- Glucose Tolerance Test, Oral [OGTT] - {IGF1 x 0' + INSU, GH, GLU x 0', 30', 60', 90', 120', 150'}
- Glucose Tolerance Test, Oral [OGTT] - {IGF1 x 0' + INSU, GLU x 0', 30', 60', 90', 120', 150'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {17OHPG x 0' + FSH, LH x -15', 0', 30', 60', 120'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {E2 x 0' + FSH, LH x -15', 0', 30', 60', 120'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {E2, 17OHPG x 0' + FSH, LH x -15', 0', 30', 60', 120'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {FSH, LH x 0', 20, 30', 60', 120'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {FSH, LH x 0', 20', 60'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {FSH, LH x -15', 0', 30', 60'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {TA x 0' + FSH, LH x -15', 0', 30', 60', 120'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {TA, 17OHPG x 0' + FSH, LH x -15', 0', 30', 60', 120'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {TA, E2 x 0' + FSH, LH x -15', 0', 30', 60', 120'}
- Gonadotropin-Releasing Hormone [GnRH/LHRH] Stimulation Test - {TA, E2, 17OHPG x 0' + FSH, LH x -15', 0', 30', 60', 120'}
- Growth Hormone Day Curve [GHDC] - {GH, GLU x 1st, 2nd, 3rd, 4th}
- Growth Hormone Profile - {GH x 0', 60', 180', 300', 480'}
- HCG Stimulation Test
- Insulin Tolerance Test [ITT] - {ACTH x 0' + CORT, GH, GLU x 0', 30', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {ACTH x 0' + CORT, GLU x 0', 30', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {ACTH x 0' + GH, GLU x 0', 30', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {CORT, GH, GLU x 0', 15', 20', 30', 45', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {CORT, GH, GLU x 0', 15', 30', 45', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {CORT, GH, GLU x 0', 30', 45', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {CORT, GH, GLU x 0', 30', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {CORT, GH, GLU x 0', 45', 60'}
- Insulin Tolerance Test [ITT] - {CORT, GLU x 0', 15', 20', 30', 45', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {CORT, GLU x 0', 30', 60', 90', 120'}
- Lactate Pyruvate Meal Challenge Test - {Lactate, Pyruvate, GLU x 0', 30', 60', 120', 180'}
- L-Dopa Stimulation Test - {GH x 0', 30', 60', 90'}
- L-Dopa Stimulation Test - {GH x 0', 30', 60', 90'+ IGF1 x 0'}
- Long Synacthen Test - {CORT x -15', 0', 30', 60', 240', 300'}
- Low Dose Short Synacthen Test [LDSSYN] - {CORT x 0', 30' 60'}
- Low Dose Short Synacthen Test [LDSSYN] - {CORT x 0', 30'}
- Metyrapone Test - { ACTH, CORT x 0', 240' }
- Noramal Saline Suppression Test - {Aldosterone, CORT, Renin x 0', 240'}
- Octreotide Suppression Test - { GH x 0', 60', 120', 180', 240', 300', 360' }
- Pentagastrin Stimulation Test - { Calcitonin x 0', 2', 3.5', 5', 10' }
- Pergonal Stimulation Test
- Peritoneal Equilibration Test [PET] - {Fluid Glucose, Fluid Creatinine x 0', 120', 240'}
- Prolactin Profile - {PRL x 0', 30', 60', 90'}
- Prolactin Profile - {PRL x 0', 30'}
- Prolonged OGTT [EGTT2] - {C-PEP, GLU x 0', 30', 60', 120', 150', 180'}
- Prolonged OGTT [EGTT2] - {C-PEP, GLU, INSU x 0', 30', 60', 120', 150', 180'}
- Prolonged OGTT [EGTT2] - {GLU, INSU x 0', 30', 60', 120', 150', 180'}
- Prolonged OGTT [EGTT2] - {GLU, INSU x 0', 60', 120', 180', 240', 300'}
- Short Synacthen Test [SST] - {17 OHPG x 0', 30', 60', 90'}
- Short Synacthen Test [SST] - {17 OHPG x 0', 30', 60'}
- Short Synacthen Test [SST] - {17-OHPG, CORT x 0', 30', 60'}
- Short Synacthen Test [SST] - {ACTH x 0' + CORT x 0', 30', 60'}
- Short Synacthen Test [SST] - {ACTH, 17OHPG x 0' + CORT x 0', 30', 60'}
- Short Synacthen Test [SST] - {CORT x 0', 20', 30', 60'}
- Short Synacthen Test [SST] - {CORT x 0', 20', 30'}
- Short Synacthen Test [SST] - {CORT x 0', 30'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {a-Subunit, TSH x 0', 30', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {fT4 ,fT3 x 0' + PRL, TSH x 0', 30', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {fT4 x 0' + PRL, TSH x 0', 30', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {fT4 x 0' + TSH x 0', 30', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {fT4, fT3 x 0' + a-Subunit, TSH x 0', 30', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {fT4, fT3 x 0' + TSH x 0', 30', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {PRL x 0' + TSH x 0', 30', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {PRL, GH, TSH x -15', 0', 20', 30', 60', 120'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {PRL, TSH x -15', 0', 20', 30', 60', 120'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {TSH x 0', 20', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {TSH x 0', 30', 60'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {TSH x -15', 0', 20', 30', 60', 120'}
- Thyrotropin-releasing Hormone [TRH] Stimulation Test - {TSH, FT4 x 0', 20', 30', 60'}
- Xylose Absorption Test - {Urine Xylose x 5-hr, Blood Xylose x 0-hr, 1-hr, 2-hr}
- Albumin, CSF
- Alpha-Fetoprotein, CSF
- Amino Acid - Glutamine, CSF
- Amino Acid - Glycine, CSF
- Amino Acid Chromatography with Quantitation, CSF
- Chloride, CSF
- Glucose, CSF
- Glutamine, CSF
- Glycine, CSF
- Human Chorionic Gonadotrophin, CSF
- Immunoglobulin A level, CSF
- Immunoglobulin A level, serum
- Immunoglobulin G level, CSF
- Immunoglobulin G level, Fluid
- Immunoglobulin G level, serum
- Immunoglobulin M level, CSF
- Immunoglobulin M level, Fluid
- Lactate Dehydrogenase [LD], CSF
- Lactic Acid [Lactate], CSF
- Lysozyme [LYSO], CFS
- Magnesium, CSF
- Netilmicin, CSF
- Neurotransmitter Metabolites, CSF
- Protein - Total, CSF
- Protein & Glucose, CSF
- Pyruvate, CSF
- 17-Oxogenic Steroids [17-Hydroxycorticosteroids], Urine
- 17-Oxosteroids [17-Ketosteroids], Urine
- 5-HIAA, Urine, Creatinine Ratio
- 5-Hydroxyindole Acetic Acid [5-HIAA], Urine
- 5-Hydroxyindole Acetic Acid [5-HIAA], Urine, 24 Hr
- 5-Hydroxyindole Acetic Acid [5-HIAA], Urine, Spot
- Acetone, Urine (GCMS)
- Acid Mucopolysaccharides - Quantitative, Urine
- Acid Mucopolysaccharides, Urine
- Acylcarnitine Profile, Urine
- Albumin & Glucose, Urine
- Albumin, Urine
- Alcohol Profile (Ethanol, Isopropanol, Methanol & Acetone), Urine
- Aldosterone, Urine
- Aluminium, Urine
- Amino Acid - Cystine, Urine
- Amino Acid Chromatography - Quantitation, Urine
- Amino Acid Chromatography - Semi-quantitative, Urine
- Amphetamine, Urine
- Amylase [Diastase], Urine
- Amylase, Urine, 24 Hr
- Amylase, Urine, Spot
- Antimony cr ratio, Urine, Spot (Profile)
- Antimony, Urine, Spot (Profile)
- Arsenic, Urine
- Arsenic, Urine, 24 Hr
- Arsenic, Urine, Spot
- Arysulphatase A & B, Urine
- Barbiturate, Urine
- Bence Jones Protein, Urine
- Benzodiazepines, Urine
- Bicarbonate, Urine
- Bilirubin - Total, Urine
- Bilirubin, Urine
- Cadmium, Urine, Spot
- Cadmium,Urine, 24 Hr
- Calcium & Creatinine, Urine, Spot
- Calcium, Urine, 24 Hr
- Calcium, Urine, 24 Hr + Creatinine, Urine, 24 Hr
- Calcium, Urine, Spot
- Camitine, Fluid
- Camitine, Urine
- Cannabinoids, Urine
- Catecholamines [Adrenaline & Noradrenaline, ME, NME, Dopamine], Urine
- Catecholamines [Adrenaline & Noradrenaline], Urine
- Catecholamines, Urine, Creatinine Ratios
- Chloride, Urine, 24 Hr
- Chloride, Urine, Spot
- Chromium cr ratio, Urine, Spot (Profile)
- Chromium, Urine, Spot (Profile)
- Chyle, Urine
- Cobalt cr Ratio, Urine, Spot (Profile)
- Cobalt, Urine, Spot (Profile)
- Cocaine, Urine
- Copper, Urine, 24 Hr
- Copper, Urine, Spot
- Coproporphyrins, Urine
- Cortisol, Urine, 24 Hr
- Cortisol, Urine, Spot
- Cortisol, Urine, Spot + Creatinine, Urine, Spot
- Creatine, Urine
- Creatinine Clearance, Urine
- Creatinine, Urine, 24 Hr
- Creatinine, Urine, Spot
- Creatinine, Urine, Spot + Phosphate, Urine, Spot
- D-Aminolevulinic Acid [D-ALA], Urine
- Diastase, Urine
- Drug Screen, Urine
- Galactose, Urine (GCMS)
- Glucose - Qualitative, Urine
- Glucose - Quantitative, Urine
- Glycosaminoglycan [MPS] - Quantitation & Typing, Urine
- Glycosaminoglycan, Urine
- Haemoglobin, Urine
- Homocysteine, Urine
- Homovanilic Acid, Urine, Creatinine Ratio
- Homovanillic Acid [HVA], Urine
- Hydroxyproline, Urine
- Imipramines, Urine
- Indocyanide Green [ICG], Urine
- Iron, Urine
- Ketone Bodies, Urine
- Lead, Urine, 24 Hr
- Lead, Urine, Spot
- Lithium, Urine
- Lysozyme [LYSO], Urine
- Magnesium, Urine, 24 Hr
- Magnesium, Urine, Spot
- Mercury, Urine
- Metabolic Screen, Urine (Colorimetric)
- Methadone, Urine
- Microalbumin, Urine, 24 Hr
- Microalbumin, Urine, Spot
- Microalbumin, Urine, Spot / Creatinine, Urine, Spot
- Myoglobin - Qualitative, Urine
- Nickel cr ratio, Urine, Spot (Profile)
- Nickel, Urine, Spot (Profile)
- Nitroprusside, Urine
- Opiates, Urine
- Organic Acid Profile, Urine
- Orotic Acid, Urine
- Orotic Acid, Urine, Creatinine Ratio
- Osmolality, Faecal
- Osmolality, Urine
- Oxalate, Urine, 24 Hr
- Oxalate, Urine, Spot
- Paraprotein, Urine (Immunofixation)
- Paraquat, Urine
- pCO2, Urine
- pH, Urine
- Phenylketone, Urine
- Phosphate, Urine, 24 Hr
- Phosphate, Urine, Spot
- Phosphoethanolamine, Urine
- Porphobilinogen, Urine (Qualitative)
- Porphobilinogen, Urine (Quantitative)
- Porphyrins, Urine
- Porphyrins, Urine, Creatinine Ratio
- Potassium, Urine, 24 Hr
- Potassium, Urine, Spot
- Pregnancy Test, Urine
- Protein & Creatinine, Urine
- Protein, Urine, 24 Hr
- Protein, Urine, Spot
- Protein, Urine, Spot + Urea, Urine, Spot + Glucose, Urine + Creatinine, Urine, Spot
- Reducing Substances, Urine
- Selenium, Urine, 24 Hr
- Selenium, Urine, Spot
- Selenium/ Creatinine ratio,Urine
- Sodium, Urine, 24 Hr
- Sodium, Urine, Spot
- Sodium, Urine, Spot + Potassium, Urine, Spot + Chloride, Urine, Spot
- Sodium, Urine, Spot + Potassium, Urine, Spot + Osmolality, Urine + Sodium [Na] + Potassium [K] + Osmolality
- Specific Gravity, Urine
- Spot Urine Iodine
- Spot Urine Iodine Creatinine Ratio
- Steroid Profile/Steroid Metabolites, Urine
- Sugar, Urine (Chromatography)
- Sulfite, Urine
- Thallium cr ratio, Urine, Spot (Profile)
- Thallium, Urine, Spot (Profile)
- Total Protein / Creatinine Ratio, Spot Urine
- Toxicology/Drug Screen, Urine
- Trichloro Compounds, Urine
- Tricyclic Anti-Depressant, Urine
- Ur. 2,4-DNPH
- Ur. Indican
- Urea, Urine, 24 Hr
- Urea, Urine, Spot
- Uric Acid, Urine, 24 Hr
- Uric Acid, Urine, Spot
- Urine amino acids, screening, ninhydrin
- Urine Metabolic Profiling
- Urobilinogen, Urine
- Uroproporphyrins - Quantitative, Urine
- Vanadium, Urine, Spot (Profile)
- Vanillyl Mandelic Acid [VMA], Urine
- Xanthurenic Acid, Urine
- Xylose Absorption Test, Urine
- Xylose, Urine
- Zinc, Urine, 24 Hr
- Zinc, Urine, Spot
- 17-Alpha Hydroxyprogesterone, Aminotic Fluid
- Alanine Aminotransferase, Fluid
- Albumin, Fluid
- Alkaline Phosphatase, Fluid
- Alpha-Fetoprotein, Fluid
- Aluminium, Fluid
- Amylase, Fluid
- Bicarbonate, Fluid
- Bilirubin - Total, Fluid
- Calcium, Fluid
- Carbon Dioxide, Fluid
- Chloride, Fluid
- Cholesterol, Fluid
- Chyle, Fluid
- Cortisol, AM, Saliva
- Cortisol, PM, Saliva
- Cortisol, Saliva
- Creatine Kinase, Fluid
- Creatinine Clearance, Fluid
- Creatinine, Fluid
- Glucose, Fluid
- Haemoglobin, Fluid
- Human Chorionic Gonadotrophin, Fluid
- Immunoglobulin A level, Fluid
- Lactate Dehydrogenase [LD], Fluid
- Lactate, Fluid
- Lysozyme [LYSO], Fluid
- Magnesium, Fluid
- pH, Cardioplegic Solution
- pH, Fluid
- Phosphate - Inorganic, Fluid
- Potassium, Cardioplegic Solution
- Potassium, Fluid
- Protein - Total, Fluid
- Renin, Fluid
- Sodium, Faecal
- Sodium, Fluid
- Triglycerides, Fluid
- Urea, Fluid
- Uric Acid, Fluid
- Calculus Analysis
- Copper, Tissue
- Creatine metabolism in CSF
- Creatine metabolism in spot urine
- Faecal Calprotectin
- Gall Stone Analysis
- Gastric Analysis - Basic Acid Output
- Gastric Analysis - Free Gastric Acid
- Gastric Analysis - Peak Acid Output
- Iron, Tissue
- Occult Blood, Faeces - Qualitative Test
- Osmolality, Fluid
- pH, Faecal
- pH, Gastric Content
- Porphyrin Profiling, Faecal
- Potassium, Faecal
- Renal Stone Analysis
- Stercobilinogen, Faeces - Qualitative Test
- Sugar, Faecal (Chromatography)
- Toxicology Screen, Gastric Content
- Anti-A Titre - IgG
- Anti-B Titre -IgG
- Blood Component Request - New Case
- Blood Component Request - New Case & Blood Component, per Unit
- Blood Component Request - Old Case
- Blood Component, per Unit
- Blood Grouping - ABO and RhD
- Blood Grouping - ABO and RhD
- Blood Grouping - ABO and RhD & Blood Component, per Unit
- Blood Grouping - ABO Anomaly Investigation
- Cold Agglutinins Screen
- Cold Agglutinins Screen
- Cold Agglutinins Titre
- Coomb's Test, Direct [Direct Antiglobulin Test]
- Coomb's Test, Direct [Direct Antiglobulin Test] + Anti-Complement + Anti-IgG + Red Cell Antibody Screening and Identification
- Coomb's Test, Indirect [Indirect Antiglobulin Test, IAT]
- Crossmatch, per Unit
- Donath-Landsteiner Test
- Glutamine, CSF x2 + Blood Component Request - New Case (Profile)
- Immunohaematology Workup, Post-Bone Marrow Transplant
- Immunohaematology Workup, Pre-Bone Marrow Transplant - Donor
- Immunohaematology Workup, Pre-Bone Marrow Transplant - Recipient
- Investigation of Transfusion Reaction, without Culture
- Paternity Test (Exclusion by Red Cell Phenotyping), per Person
- Red Cell Antibody Screen
- Red Cell Antibody Screening and Identification
- Rh D Typing
- Rh D Typing x 2
- Rh Phenotyping
- Rhesus Antibody Titre
- Serology Report
- Type & Screen
- Type & Screen - Baby Blood Only
- Type & Screen - Baby Blood Only + Coomb's Test, Direct [Direct Antiglobulin Test] + Anti-A Titre - IgG + Anti-B Titre -IgG
- Type & Screen - New Case
- Type & Screen - Old Case
- Type & Screen for Mother & Baby - New Case
- Type & Screen for Mother & Baby - Old Case
- Blood Film Examination
- Complete Blood Count [CBC]
- Complete Blood Count [CBC] & Erythrocyte Sedimentation Rate [ESR]
- Complete Blood Count [CBC] + Blood Film Examination
- Complete Blood Count [CBC] + Erythrocyte Sedimentation Rate [ESR] + Reticulocyte Count [Retic]
- Complete Blood Count [CBC] + Reticulocyte Count [Retic]
- Eosinophil Count
- Erythrocyte Sedimentation Rate [ESR]
- Glucose 6-Phosphate Dehydrogenase [G6PD] - Qualitative
- Haemosiderin, Urine
- Malaria Parasites Examination
- Microfilariae Examination
- Monospot Test
- Plasma Haemoglobin
- Reticulocyte Count [Retic]
- Semen Analysis for Sperm Count and Morphology
- Activated Partial Thromboplastin Time [APTT]
- Activated Protein C Resistance
- Anti-Thrombin Assay
- Bleeding Time
- Coagulation Factor Assay
- Coagulation Factor Assay - Factor II
- Coagulation Factor Assay - Factor IX
- Coagulation Factor Assay - Factor V
- Coagulation Factor Assay - Factor VII
- Coagulation Factor Assay - Factor VIII
- Coagulation Factor Assay - Factor X
- Coagulation Factor Assay - Factor XI
- Coagulation Factor Assay - Factor XII
- Coagulation Factor Assay, per Assay
- Coagulation Factor IX Inhibitor Assay
- Coagulation Factor VIII Inhibitor Assay
- Coagulation Factor XIII Screen
- Coagulation Inhibitor Assay
- Coagulation Inhibitor Screening Tests
- Coagulation Inhibitor Screening Tests + Coagulation Inhibitor Assay
- D-Dimer - Qualitative
- D-Dimer - Quantitative
- Dilute Russel Viper Venom Test
- Euglobulin Lysis Time
- Factor 11 assay
- Factor 8 assay
- Factor 9 assay
- Fibrin Degradation Products
- Fibrin Monomer (Haemagglutination)
- Fibrin Monomer (Protamine Sulphate Test)
- Fibrinogen Quantitation
- Heparin Assay [Anti-Xa Activity]
- Heparin-PF4 Antibodies
- Kaolin Clotting Time
- Lupus Anticoagulant
- Lupus Anticoagulant Study
- Platelet Function Test
- Protein C
- Protein C, Anti-Thrombin Assay, Activated Protein C Resistance, Protein S (Total & Free), Lupus Anticoagulant
- Protein S - Free
- Protein S - Total and Free
- Prothrombin Time [PT/INR]
- Prothrombin Time [PT/INR] & APTT
- Prothrombin Time [PT/INR] & APTT & Fibrinogen
- Prothrombin Time [PT/INR] & APTT & Fibrinogen & D-Dimer
- Ristocetin-induced Platelet Aggregation (RIPA)
- Thrombin Time
- Thrombin Time & Protamine Sulphate test
- von Willebrand Antigen Assay
- von Willebrand Disease Investigation
- vWF:Antigen
- Acidified Glycerol Lysis Test
- Alpha globin genotype (Profile)
- Autohaemolysis Test
- Beta globin genotype (Profile)
- Globin chian electrophoresis
- Haemoglobin A1c
- Haemoglobin H Inclusion Bodies
- Haemoglobin Heat Instability Test
- Haemoglobin Pattern
- Haemoglobin S Sickling Test
- Haemoglobin S Solubility Test
- Ham’s Test
- HbP
- Heinz Bodies
- Kleihauer Test
- Methaemoglobin Assay
- Osmotic Fragility Test
- Pyruvate Kinase Screen
- Schumm's Test [Methaemalbumin]
- Serum B12
- Sucrose Lysis Test
- Sulphaemoglobin
- Unstable Haemoglobin
- Vitamin B12, Serum Folate and Red Cell Folate
- Blood Film Review
- Bone Marrow Aspirate Cytology
- Bone Marrow Slide Review
- CD3 Viability by Flow Cytometry
- CD34+ Cells Assay
- CD34+ Cells Assay x3 (Profile)
- Cytochemical Stain - Acid Phosphatase
- Cytochemical Stain - Acid Phosphatase with Tartrate
- Cytochemical Stain - Chloroacetate Esterase
- Cytochemical Stain - Dual Esterase
- Cytochemical Stain - Myeloperoxidase
- Cytochemical Stain - Non-specific Esterase
- Cytochemical Stain - Non-specific Esterase with Fluoride
- Cytochemical Stain - PAS
- Cytochemical Stain - Sudan Black
- Cytochemical Staining Profile
- Cytochemical Staining, per Stain
- DNA Ploidy
- EMA-binding to hereditary spherocytosis red cells
- Erythropoietin
- Human platelet antigen genotyping
- Immune Marker - CD10
- Immune Marker - CD103
- Immune Marker - CD117
- Immune Marker - CD11b
- Immune Marker - CD11c
- Immune Marker - CD13
- Immune Marker - CD138
- Immune Marker - CD14
- Immune Marker - CD15
- Immune Marker - CD16
- Immune Marker - CD19
- Immune Marker - CD1a
- Immune Marker - CD2
- Immune Marker - CD20
- Immune Marker - CD22
- Immune Marker - CD23
- Immune Marker - CD25
- Immune Marker - CD3
- Immune Marker - CD30
- Immune Marker - CD33
- Immune Marker - CD34
- Immune Marker - CD38
- Immune Marker - CD4
- Immune Marker - CD41
- Immune Marker - CD42b
- Immune Marker - CD45
- Immune Marker - CD5
- Immune Marker - CD55
- Immune Marker - CD56
- Immune Marker - CD57
- Immune Marker - CD58
- Immune Marker - CD59
- Immune Marker - CD61
- Immune Marker - CD7
- Immune Marker - CD79a
- Immune Marker - CD8
- Immune Marker - Cyclin D1
- Immune Marker - FMC-7
- Immune Marker - Glycophorin A
- Immune Marker - HC2
- Immune Marker - HLA-DR
- Immune Marker - Tdt
- Immunophenotyping Profile
- Immunophenotyping, per Cell Marker
- Lymphocytes CD4 & CD8 - 5 Markers
- Neutrophil Alkaline Phosphatase [NAP]
- Paroxysmal Nocturnal Hemoglobinuria [PNH] Diagnosis (Flow Cytometry)
- Platelet antibody by direct MAIPA method
- Platelet antibody by indirect MAIPA method
- Conventional Cytogenetic Studies, Blood / Bone Marrow
- Conventional Cytogenetic Studies, Solid Tumour
- 11q23, Leukaemia and Lymphomas, Chromosomal Abnormality (FISH)
- 1p/19q, High Grade Gliomas, Deletion Detection (FISH)
- 1p19q status FISH test
- A gamma promoter - 196(G to T) detection
- ALK, Lung Carcinoma, Translocation Detection (FISH)
- ALL Minimal Residual Disease (MRD) marker identification (NGS & qPCR) (Profile)
- ALL Minimal Residual Disease (MRD) marker identification (NGS) (Profile)
- ALL Minimal Residual Disease (MRD) marker identification (qPCR & Equipment) (Profile)
- ALL Minimal Residual Disease (MRD) qPCR follow up
- AML1-ETO, Acute Myeloid Leukaemia, Translocation Detection (FISH)
- AML1-ETO, Acute Myeloid Leukaemia, Translocation Detection (PCR)
- AML-MRD by ddPCR (droplet digital PCR)
- BCL1-IGH, Mantle Cell Lymphoma, Translocation Detection (PCR)
- BCL-2,Lymphoma, Translocation Detection (FISH)
- BCL2-IGH, B-Cell Lymphoma, Translocation Detection (FISH)
- BCL2-IGH, B-Cell Lymphoma, Translocation Detection (PCR)
- BCL2-IGH, B-Cell Lymphoma, Translocation Detection at MBR & mcr (PCR)
- BCL2-IGH, B-Cell Lymphoma, Translocation Detection at MBR (PCR)
- BCL-6, Lymphoma, Translocation Detection (FISH)
- BCR INI1, Sarcoma, Deletion Detection (FISH)
- BCR-ABL, Chronic Myeloid Leukaemia, Translocation Analysis (qPCR, Multiple Targets)
- BCR-ABL, Chronic Myeloid Leukaemia, Translocation Analysis (qPCR, Single Target)
- BCR-ABL1 - p190, Chronic Myeloid Leukaemia, Translocation Analysis (PCR)
- BCR-ABL1 - p190, p210, b2a3, b3a3, e19a3, Chronic Myeloid Leukaemia, Translocation Analysis (PCR)
- BCR-ABL1 - p190+p210, Chronic Myeloid Leukaemia, Translocation Analysis (PCR)
- BCR-ABL1 - p210, Chronic Myeloid Leukaemia, Translocation Analysis (PCR)
- BCR-ABL1, Chronic Myeloid Leukaemia, Translocation Analysis (FISH)
- BRAF V600E mutation by ARMS and HRM for hairy cell leukemia
- Calreticulin mutation for myeloproliferative neoplasm
- CBFB::MYH11 ddPCR
- CBFB-MYH11, Acute Myeloid Leukaemia, Translocation Detection (FISH)
- CBFB-MYH11, Acute Myeloid Leukaemia, Translocation Detection (PCR)
- CCND1-IGH, Mantle Cell Lymphoma, Translocation Detection (FISH)
- CCND1-IGH, Mantle Cell Lymphoma, Translocation Detection (PCR)
- CEBPA mutation detection for acute myeloid leukaemia
- Chinese delta beta thalassaemia mutation detection
- Chromosome Fluorescence In Situ Hybridization for Various Solid Tumours (FISH)
- Chronic Lymphocytic Leukaemia, Metaphase Study (FISH, Panel)
- CML BCR-ABL1 Kinase Domain Mutation Detection
- c-MYC, Lymphoma, Translocation Detection (FISH)
- COL1A1-PDGFB, Dermatofibrosarcoma Protuberans [DFSP], Translocation Detection, (FISH)
- CSF3R mutation detection for chronic neutrophilic leukaemia
- DICER1 RNase IIIa and IIIb domains Sanger sequencing
- E2A-PBX1, Acute Lymphoblastic Leukaemia, Translocation Detection (FISH)
- E2A-PBX1, Acute Lymphoblastic Leukaemia, Translocation Detection (PCR)
- EGFR Mutation Test on Liquid Biopsies
- EGFR, Lung Carcinoma, Mutation Analysis
- ERBB2 [HER2], Breast Carcinoma, Gene Amplification (CISH)
- ERBB2 [HER2], Breast Carcinoma, Gene Amplification (FISH)
- ETV6, Tumour, Translocation Detection (FISH)
- ETV6-PDGFRB, Chronic Myelomonocytic Leukaemia, Translocation Detection (PCR)
- EWS, Solid Tumour, Translocation Detection (FISH)
- EWS-ATF1, Clear Cell Sarcoma Gene, Translocation Detection (PCR)
- EWS-FLI1, Ewing's Sarcoma/PNET,Translocation Detection (PCR)
- EWS-WT1, Desmoplastic Small Round Cell Tumour, Translocation Detection (PCR)
- FIP1L1-PDGFRA, Chronic Eosinophilic Leukaemia, Translocation Detection (FISH)
- FIP1L1-PDGFRA, Chronic Eosinophilic Leukaemia, Translocation Detection (PCR)
- FISH / Dual-ISH for HER2 gene amplification (Gastric)
- FLT3, Acute Myeloid Leukemia, Exon 14 ITD Mutation Detection (Sequencing)
- FUS, Sarcoma, Translocation Detection (FISH)
- G gamma promoter - 158(G to T) detection
- IGH and IGK rearrangement detection by NGS
- IgH Fr2 and Fr3 Gene Rearrangement (PCR)
- IgH Gene Rearrangement (PCR)
- IGH, Lymphoma, Translocation Detection (FISH)
- IGH-FGFR3, Plasma Cell Disorder, Translocation Detection (FISH)
- IGH-MAF, Plasma Cell Disorder, Translocation Detection (FISH)
- IGH-MYC, B-Cell Lymphoma, Translocation Detection (FISH)
- IGHV Somatic hypermutation detection by NGS
- IGK [Kappa] and IGL [Lambda] mRNA (ISH)
- IHC Antibody Cocktail Assay
- IHC ROS-1 Test
- IHC TRK Test
- JAK2 exon 12 mutation detection for myeloproliferative neoplasm
- JAK2 V617F, Myeloproliferative Disorders, Mutation Detection (PCR)
- JAK2 V617F, Myeloproliferative Disorders, Mutation Detection (PCR) + JAK2, Myeloproliferative Disorders, Mutation Detection (Sequencing)
- JAK2 V617F, Myeloproliferative Disorders, Mutation Detection (Screening)
- JAK2, Myeloproliferative Disorders, Mutation Detection (Sequencing)
- Kappa and Lambda mRNA (ISH)
- KIT, Acute Myeloid Leukaemia [AML]/Gastrointestinal Stromal Tumour [GIST], Mutation Analysis (PCR & sequencing)
- KIT, Acute Myeloid Leukaemia [AML]/Gastrointestinal Stromal Tumour [GIST], Mutation Analysis (PCR)
- KIT, Acute Myeloid Leukaemia [AML]/Gastrointestinal Stromal Tumour [GIST], Mutation Analysis (Sequencing)
- KRAS, Adenocarcinomas and Mucinous Tumours, Mutation Analysis (PCR & Sequencing)
- KRAS, Adenocarcinomas and Mucinous Tumours, Mutation Analysis (PCR-RFLP)
- KRAS, Adenocarcinomas and Mucinous Tumours, Mutation Analysis (PCR-RFLP) & (Sequencing)
- KRAS, Adenocarcinomas and Mucinous Tumours, Mutation Analysis (Sequencing)
- MDM2, Liposarcoma, Gene Amplification (FISH)
- MEN1, Multiple Endocrine Neoplasia Type 1, Gene Analysis (Sequencing)
- MENI, Multiple Endocrine Neoplasia type, (PCR & DNA sequencing)
- Methylation profiling
- MGMT, Glioblastoma, Promoter Methylation Assay for Treatment Selection (PCR & sequencing)
- MGMT, Glioblastoma, Promoter Methylation Assay for Treatment Selection (PCR)
- MLL-AF4, Acute Lymphoblastic Leukaemia, Translocation Detection (PCR)
- MPL mutation detection for meyloproliferative neoplasm
- Multiplex PCR to detect --(THAI) and --(FIL) deletions
- Multiplex PCR to detect alpha globin gene amplification (anti-3.7 and anti-4.2)
- Multiplex PCR to detect SEA deletion and single alpha globin gene deletions (3.7kb and 4.2kb)
- Multiplex qualitative RT-PCR for p190(e1a2), p210(e13a2 and e14a2) and JAK2 p.V617F mutation with 2 confirmation PCRs
- Mutation detection of HbCS, HbQS and codon 30 (GAG) deletion
- MYC-IgH, Lymphoma, Fusion Detection (FISH)
- MYD88 mutation detection for lymphoplasmacytic lymphoma
- Myeloid & Lymphoid DNA panel, NGS
- Myeloid & Lymphoid RNA panel - Profile test 2: RT-PCR Sanger Sequencing
- Myeloid & Lymphoid RNA panel, profile test 1: NGS
- Myeloma, Interphase Study (FISH, Panel)
- Myeloma/CLL Panel - ATM, CEP12, 13q14, 13q34, TP53 (FISH)
- Myleoid & Lymphoid RNA panel, Profile test 1.NGS 2. RT-PCR Sanger Sequencing (Profile)
- MYOD1 L122R Sanger sequencing
- Next Generation Sequencing (NGS) RNA Fusion Panel
- NOTCH1/FBXW7 hotspots Sanger Sequencing
- NPM1 and FLT-1TD mutation for acute myeloid leukaemia
- NPM1 ddPCR
- NPM1, Acute Myeloid Leukaemia, Exon 12 Insertion Detection (Sequencing)
- NPM-ALK, Anaplastic Large-Cell Lymphoma, Translocation Detection (PCR)
- PAX3-FKHR, Alveolar Rhabdomyosarcoma, Translocation Detection (PCR)
- PAX7-FKHR, Alveolar Rhabdomyosarcoma, Translocation Detection (PCR)
- PDGFRA, Gastrointestinal Stromal Tumour [GIST], Mutation Analysis (PCR & sequencing)
- PD-L1 IHC Test
- PIK3CA gene mutation test
- PML-RARA, Acute Promyelocytic Leukaemia, Translocation Detection (FISH)
- PML-RARA, Acute Promyelocytic Leukaemia, Translocation Detection (PCR)
- Quantitative PCR for RUNX1-RUNX1T1 transcript for acute myeloid leukaemia
- RET, Multiple Endocrine Neoplasia Type 2, Gene Analysis (Sequencing)
- RNA pan-cancer panel - Profile test 1: Next Generation Sequencing (NGS)
- RNA pan-cancer panel - Profile test 2: RT-PCR Sanger Sequencing
- RNA pan-cancer panel, Profile test 1.NGS 2. RT-PCR Sanger Sequencing (Profile)
- ROS1 FISH test
- SDHAF2, Familial paraganglioma / phaeochromocytoma, (PCR & DNA sequencing)
- SDHB, Familial paraganglioma, (PCR & DNA sequencing)
- SDHC, Familial paraganglioma / phaeochromocytoma, (PCR & DNA sequencing)
- SDHD, Familial paraganglioma, (PCR & DNA sequencing)
- SETBP1 mutation detection for MPN and MDS
- Southeast Asian (SEA) HPFH deletion (Vietnamese deletion)
- SS18, Synovial Sarcoma, Translocation Detectionn (FISH)
- SYT-SSX, Synovial Sarcoma, Translocation Detection (PCR)
- TCR-Beta and -Gamma Gene Rearrangement Detection (PCR & sequencing) (Profile)
- TCR-Beta and -Gamma Gene Rearrangement Detection (PCR)
- TCR-Beta Gene Rearrangement Detection (PCR)
- TCR-Gamma Gene Rearrangement Detection (PCR)
- TEL-AML1, Acute Lymphoblastic Leukaemia, Translocation Detection (FISH)
- TEL-AML1, Acute Lymphoblastic Leukaemia, Translocation Detection (PCR)
- TH, Neuroblastoma, Gene Detection (PCR)
- TP53 [p53] Mutation Detection (PCR-SSCP)
- Translocation Detection in Leukaemia and Lymphoma (PCR)
- Translocation Detection in Solid Tumour (PCR & sequencing) & Targeted Screening for One Mutation (Sequencing) (Profile)
- Translocation Detection in Solid Tumour (PCR)
- TruSight Oncology 500 - consumables
- TruSight Oncology 500 - Profile Test
- TruSight Oncology 500 - without consumables
- VHL, Familial paraganglioma, (PCR & DNA sequencing)
- WT1, Wilms Tumour / Congenital Nephrotic Syndrome / Drash Syndrome / Frasier Syndrome, Gene Analysis (Sequencing)
- ZNF198-FGFR1, 8p11 Myeloproliferative Syndrome, Translocation Detection (PCR)
- A gamma promoter sequencing
- ABCB11, Progressive Familial Intrahepatic Cholestasis Type 2, Gene Analysis (Sequencing)
- ABCB4, Progressive Familial Intrahepatic Cholestasis Type 3, Gene Analysis (Sequencing)
- ABCC8, Neonatal Diabetes or Hyperinsuliniemic Hypoglycemia of Infancy, Gene Analysis (Sequencing)
- ABCD1, X-Linked Adrenoleukodystrophy, Gene Analysis (Sequencing)
- ABCG5, Phytosterolaemia, Gene Analysis (Sequencing)
- ABCG8, Phytosterolaemia, Gene Analysis (Sequencing)
- ACADVL, Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Gene Analysis (Sequencing)
- ACAT1, Acetoacetyl-CoA Thiolase Deficiency / 3-Ketothiolase Deficiency
- AGL, Glycogen Storage Disease Type III, Gene Analysis (Sequencing)
- AGXT, Primary Hyperoxaluria Type I, Gene Analysis (Sequencing)
- AIRE,Autoimmune polyglandular disease type I,(PCR & DNA sequencing)
- Alpha globin gene cluster screening by alpha MLPA (Multiplex Ligation-dependent Probe Amplification)
- Alpha Plus Thalassaemia (-a3.7 and aaa. anti-3.7)
- Alpha Plus Thalassaemia (-a4.2)
- Alpha Plus Thalassaemia for SEA Deletion and Single a-Globin Gene Deletion, 3.7kb & 4.2kb (Multiplex PCR)
- Alpha Thalassaemia (a-Globin Gene Sequencing)
- Alpha Thalassaemia (Hb Constant Spring and Hb Quong Sze Mutation)
- Alpha Thalassaemia Test Panel
- Alpha Zero Thalassaemia for 5 Common Deletions: -SEA, -(a)20.5, --MED, --FIL, and --THAI (PCR)
- ALPL, Hypophosphatasia, Gene Analysis (Sequencing)
- AML / ALL Gene Fusion real-time PCR
- AMT, Non-Ketotic Hyperglycaemia (T Protein), Gene Analysis (Sequencing)
- APOA5, Familial Dyslipidaemia, Gene Analysis (Sequencing)
- APOC2, Familial Dyslipidaemia, Gene Analysis (Sequencing)
- APOE, Disbetalipoproteinaemia, Gene Analysis (PCR-RFLP)
- APOE, Disbetalipoproteinaemia, Gene Analysis (Sequencing)
- AQP2, Autosomal dominant or recessive nephrogenic diabetes insipidus, (PCR & DNA sequencing)
- AR, Androgen Insensitivity Syndrome, Gene Analysis (PCR)
- AR, Kennedy Disease, Spinobulbar Muscular Dystrophy, Gene Analysis (PCR)
- AR, Kennedy Disease, Spinobulbar Muscular Dystrophy, Gene Analysis (Sequencing)
- ARG1, Arginase Deficiency, Gene Analysis (Sequencing)
- ARM, Aromatase deficiency, (PCR & DNA sequencing)
- ARSA, Metachromatic Leucodystrophy, Gene Analysis (Sequencing)
- ARSB, Mucopolysaccharidosis Type VI, Gene Analysis (Sequencing)
- ARX, X-linked Mental Retardation / Aristaless-related Homeobox, Gene Analysis (Sequencing)
- ASL, Argininosuccinate Lyase Deficiency, Gene Analysis (Sequencing)
- ASS1, Argininosuccinate Synthetase Deficiency, Gene Analysis (Sequencing)
- ATN1, Dentatorubral Pallidoluysian Atrophy, Gene Analysis (PCR)
- ATN1, Dentatorubral Pallidoluysian Atrophy, Gene Analysis (PCR)
- ATN1, Dentatorubral-Pallidoluysian Atrophy, Gene Analysis (Sequencing)
- ATP7A, Menkes Disease, Gene Analysis (Sequencing)
- ATP7B, Wilson Disease, Gene Analysis (Sequencing)
- ATP8B1, Progressive Familial Intrahepatic Cholestasis Type 1, Gene Analysis (Sequencing)
- ATXN1, Spinocerebellar Ataxia 1, Gene Analysis (PCR)
- ATXN10, Spinocerebellar Ataxia 10, Gene Analysis (PCR)
- ATXN2, Spinocerebellar Ataxia 2, Gene Analysis (PCR)
- ATXN3, Spinocerebellar Ataxia 3, Gene Analysis (PCR)
- ATXN3, Spinocerebellar Ataxia 3, Gene Analysis (TP PCR)
- ATXN7, Spinocerebellar Ataxia 7, Gene Analysis (PCR)
- ATXN8OS, Spinocerebellar Ataxia 8, Gene Analysis (PCR)
- ATXN8OS, Spinocerebellar Ataxia 8, Gene Analysis (TP PCR)
- Atypical Rett Syndrome, Gene Analysis (MLPA)
- AVPR2, X-linked nephrogenic diabetes insipidus, (PCR & DNA sequencing)
- BAAT, Familial Hypercholanaemia, Gene Analysis (Sequencing)
- BAG3, BAG3-Related Myofibrillar Myopathy, Gene Analysis (Sequencing)
- BCHE, Butyrylcholinesterase Deficiency, Gene Analysis (Sequencing)
- BCKDHA, Maple Syrup Urine Disease, Gene Analysis (Sequencing)
- BCKDHB, Maple Syrup Urine Disease, Gene Analysis (Sequencing)
- BCR-ABL1 p190 ddPCR
- Beta globin gene cluster screening by beta MLPA (Multiplex Ligation-dependent Probe Amplification)
- Beta Thalassaemia (b-Globin Gene Sequencing)
- Beta Thalassaemia, Screening for Common Mutations
- BSND, Bartter Syndrome Type 4, Gene Analysis (Sequencing)
- C10orf2, Progressive External Ophthalmoplegia, Gene Analysis (Sequencing)
- C9orf72 repeat expansion testing
- CACNA1A, Spinocerebellar Ataxia 6, Gene Analysis (PCR)
- CAPN3, Calpainopathy / Limb Girdle Muscular Dystrophy 2A, Gene Analysis (Sequencing)
- Cardiac panel cost (Profile)
- Cardiac Panel- Profile test 1: Next Generation Sequencing, NGS (Profile)
- CASQ2, Catecholaminergic Polymorphic Ventricular Tachycardia / Calsequestrin 2, Gene Analysis (Sequencing)
- CAV3, Caveolinopathy / Limb Girdle Muscular Dystrophy 1C, Gene Analysis (Sequencing)
- CBS, Homocystinuria, (PCR & DNA sequencing)
- CDC73, Familial Isolated Hyperparathyroidism, Gene Analysis (Sequencing)
- CDC73, Primary hyperparathyroidism or hyperparathyroidism-jaw tumour syndrome, (PCR & DNA sequencing)
- CDH1, Hereditary Diffuse Gastric Cancer, Gene Analysis (Sequencing)
- CH25H, Cholesterol 25-Hydroxylase Deficiency, Gene Analysis (Sequencing)
- Childhood cancer and Vascular Anomalies NGS panel
- Chinese Gg(Agdb)0 Thalassaemia Test
- CHIT1, Chitotriosidase Deficiency, Gene Analysis (Sequencing)
- CLCNKB, Bartter Syndrome Type 3, Gene Analysis (Sequencing)
- CNBP, Myotonic Dystrophy Type 2, Gene Analysis (PCR)
- CNBP, Myotonic Dystrophy Type 2, Gene Analysis (TP PCR)
- COL1A1, Osteogenesis Imperfecta Types I, II, III, IV / Ehlers-Danlos Syndrome Types I, VIIA, Gene Analysis (Sequencing)
- COL1A2, Osteogenesis Imperfecta Types II, III, IV / Ehlers-Danlos Syndrome Cardiac Valvular Form and Type VIIB, Gene Analysis (Sequencing)
- CPS, Carbamyol-phosphate synthetase deficiency, (PCR & DNA sequencing)
- CPS1, Carbamyol-Phosphate Synthetase Deficiency, Gene Analysis (Sequencing)
- CPT2, Carnitine Palmitoyltransferase II Deficiency, Gene Analysis (Sequencing)
- CPT2, Thermolabile Carnitine Palmitoyltransferase II Variants, Gene Analysis (Sequencing)
- CRTAP, Osteogenesis Imperfecta Type VII, Gene Analysis (Sequencing)
- CYB5A, Cytochrome b5 deficiency, (PCR & DNA sequencing)
- CYP11A1, 46XY Sex Reversal and Adrenal Insufficiency, Gene Analysis (Sequencing)
- CYP17A, 17-alpha hydroxylase deficiency, (PCR & DNA sequencing)
- CYP21A2, 21-Hydroxylase Deficiency, Gene Analysis (MLPA)
- CYP21A2, 21-Hydroxylase Deficiency, Gene Analysis (Sequencing)
- CYP27A1, Cerebrotendinous Xanthomatosis, Gene Analysis (Sequencing)
- CYP3A5*3/*6/*7 genotyping
- CYP7B1, Hereditary Spastic Paraplegia 5A, Gene Analysis (Sequencing)
- DBT, Maple Syrup Urine Disease, Gene Analysis (Sequencing)
- DDC, Aromatic L-Amino Acid Decarboxylase Deficiency, Gene Analysis (Sequencing)
- Delta globin gene sequencing
- Dihydropyrimidine Dehydrogenease Deficiency Genetic Test (DPYD)
- DLD, Dihydrolipoamide Dehydrogenase Deficiency, Gene Analysis (Sequencing)
- DMPK, Myotonic Dystrophy Type 1, Gene Analysis (AmplideX PCR)
- DMPK, Myotonic Dystrophy Type 1, Gene Analysis (PCR)
- DMPK, Myotonic Dystrophy Type 1, Gene Analysis (TP PCR)
- DNAI1, Primary Ciliary Dyskinesia, Gene Analysis (Sequencing)
- DPYD, Dihydropyrimidine Dehydrogenease Deficiency / Pharmacogenetic Test for Irinotecan, Gene Analysis (Sequencing)
- Early Infantile Epileptic Encephalopathy (EIEE) panel - Profile test 1: Next Generation Sequencing, NGS (Profile)
- EIEE panel cost (Profile)
- ELANE, Congenital ELANE-related Neutropenia, Gene Analysis (Sequencing)
- EMD, Emery-Dreyfuss Muscular Dystrophy, Gene Analysis (Sequencing)
- ETFA, Multiple Acyl-CoA Dehydrogenase Deficiency / Glutaric Aciduria Type 2A, Gene Analysis (Sequencing)
- ETFB, Multiple Acyl-CoA Dehydrogenase Deficiency / Glutaric Aciduria Type 2B, Gene Analysis (Sequencing)
- ETFDH, Multiple Acyl-CoA Dehydrogenase Deficiency / Glutaric Aciduria Type 2C, Gene Analysis (Sequencing)
- EVC, Ellis van Creveld Syndrome, Gene Analysis (Sequencing)
- EVC2, Ellis van Creveld Syndrome 2, Gene Analysis (Sequencing)
- Exome reanalysis
- Factor V Leiden G1691A Mutation Screening
- Factor VIII Gene (Sequencing)
- Factor VIII Gene Intron 22 and Intron 1 Inversions (PCR)
- Factor VIII Gene Single Exon for Female Relatives of Patients with Known Mutation (Sequencing)
- FAH, Tyrosinaemia Type 1, Gene Analysis (Sequencing)
- FC1, Progressive familial intrahepatic cholestasis type 1, (PCR & DNA sequencing)
- FGFR2, Fibroblast Growth Factor Receptor 2-Related Craniosynostosis Syndrome, Gene Analysis (Sequencing)
- FGFR3 hotspot mutation (p.G380R and p.N540K), Gene Analysis (Sequencing)
- FGFR3, Fibroblast Growth Factor Receptor 3 / Thanatophoric Dysplasia / Crouzon Syndrome, Gene Analysis (Sequencing)
- FIC, Progressive familial intrahepatic cholestasis type 2, (PCR & DNA sequencing)
- FKBP10, Osteogenesis Imperfecta Type VI, Gene Analysis (Sequencing)
- FKRP, Limb Girdle Muscular Dystrophy 2I (Fukutin), Gene Analysis (Sequencing)
- FMR1, Fragile X syndrome, Gene Analysis (AmplideX mPCR)
- FMR1, Fragile X syndrome, Gene Analysis (PCR)
- FMR1, Fragile X syndrome, Gene Analysis (TP PCR)
- FXN, Friedriech Ataxia, Gene Analysis (LR-PCR)
- FXN, Friedriech Ataxia, Gene Analysis (PCR)
- G gamma promoter sequencing
- G6PC, Glycogen storage disease type 1a, (PCR & DNA sequencing)
- G6PC, Glycogen Storage Disease Type IA, Gene Analysis (Sequencing)
- G6PT1, Glycogen storage disease type 1b, (PCR & DNA sequencing)
- G6PT1, Glycogen Storage Disease Type IB, Gene Analysis (Sequencing)
- GA1, Glutaric acidemia type I, (PCR & DNA sequencing)
- GAA, Glycogen Storage Disease Type II, Gene Analysis (Sequencing)
- GAA, Pompe disease, (PCR & DNA sequencing)
- GABRG2, Severe Myoclonic Epilepsy of Infancy, Gene Analysis (Sequencing)
- GALNS, Mucopolysaccharidosis Type IV A, Gene Analysis (Sequencing)
- GAMT, Guanidinoacetate Methyltransferase Deficiency, Gene Analysis (Sequencing)
- GATA3, GATA3-related hypoparathyroidism, sensorineural deafness and renal disease, (PCR & DNA sequencing)
- GATM, Arginine:Glycine Amidinotransferase Deficiency, Gene Analysis (Sequencing)
- GCDH, Glutaric Aciduria Type 1, Gene Analysis (Sequencing)
- GCH1, Guanosine Triphosphate Cyclohydrolase I Deficiency / Segawa Disease, Gene Analysis (Sequencing)
- GCK, Maturity onset diabetes of the young, type II, (PCR & DNA sequencing)
- GCSH, Non-Ketotic Hyperglycaemia (H Protein), Gene Analysis (Sequencing)
- GJB1, X-linked Charcot-Marie-Tooth Disease, Gene Analysis (Sequencing)
- GJB2, Nonsyndromic Congenital Deafness, Gene Analysis (Sequencing)
- GJB3, Nonsyndromic Congenital Deafness, Gene Analysis (Sequencing)
- GJB6, Nonsyndromic Congenital Deafness, Gene Analysis (Sequencing)
- GLA, Fabry Disease, Gene Analysis (Sequencing)
- GLB1, GM1-Gangliosidosis, Gene Analysis (Sequencing)
- GLDC, Non-Ketotic Hyperglycaemia (P protein), Gene Analysis (Sequencing)
- GLRA1, Hyperekplexia, Gene Analysis (Sequencing)
- GLUD1, Hyperinsulinism Hyperammonaemia Syndrome, Gene Analysis (Sequencing)
- GNAS, Albright hereditary osteodystrophy, (PCR & DNA sequencing)
- GNAS, GNAS Complex Locus Disorders / Pseudohypoparathyroidism / Albright Hereditary Osteodystrophy, Gene Analysis (Sequencing)
- GNS, Mucopolysaccharidosis Type III D, Gene Analysis (Sequencing)
- GPT, Alanine Aminotransferase Deficiency, Gene Analysis (Sequencing)
- GRHPR, Primary Hyperoxaluria Type 2, Gene Analysis (Sequencing)
- HADH, 3-Alpha-Hydroxyacyl-CoA Dehydrogenase Deficiency, Gene Analysis (Sequencing)
- HADHA, Mitochondrial Trifunctional Protein Deficiency, Gene Analysis (Sequencing)
- HADHB, Mitochondrial Trifunctional Protein Deficiency, Gene Analysis (Sequencing)
- HD, Huntington Disease, Gene Analysis (PCR)
- HD, Huntington Disease, Gene Analysis (TP PCR)
- Hereditary Blood Disease - Profile test 1: Next Generation Sequencing, NGS
- Hereditary Blood Disease - Profile test 2: Sanger Sequencing (confirmation)
- Hereditary Blood Disease, NGS & Sanger Sequencing (confirmation)
- HFE CYS282TYR/HIS63ASP, Hereditary Haemochromatosis, Mutation Screening
- HFE, Hereditary Haemochromatosis, Gene Analysis (PCR-RFLP)
- HFE, Hereditary Haemochromatosis, Gene Analysis (Sequencing)
- HGSNAT, Mucopolysaccharidosis Type III C, Gene Analysis (Sequencing)
- HLCS, Holocarboxylase Synthetase Deficiency / Multiple Carboxylase Deficiency, Gene Analysis (Sequencing)
- HMBS, Actue Intermittent Porphyria, Gene Analysis (Sequencing)
- HNF1A, Maturity onset diabetes of the young, type III, (PCR & DNA sequencing)
- HNF4A, Maturity onset diabetes of the young, type I, (PCR & DNA sequencing)
- HPFH-1,2,3,6 and SEA, Hereditary Persistence of Fetal Haemoglobin Screening
- HSD11B2, Apparent Mineralocorticoid Excess, Gene Analysis (Sequencing)
- HSD17, 17£]-hydroxysteroid dehydrogenase deficency, (PCR & DNA sequencing)
- HSD17B3, 17-Beta-Hydroxysteroid Dehydrogenase Deficency, Gene Analysis (Sequencing)
- HSD17B4, D-Bifunctional Protein Deficiency, Gene Analysis (Sequencing)
- HSD3B2, 3-Beta-Hydroxysteroid Dehydrogenase Deficiency, Gene Analysis (Sequencing)
- HSD3B7, 3-Beta-Hydroxysteroid Oxidoreductase Deficiency, Gene Analysis (Sequencing)
- IDA, Mucopolysaccharidosis Type I, (PCR & DNA sequencing)
- IDS, Mucopolysaccharidosis Type II, Gene Analysis (Sequencing)
- IDUA, Mucopolysaccharidosis Type IH, Gene Analysis (Sequencing)
- IFNGR1, Interferon Gamma Receptor 1 / Susceptibility to Mycobacterium tuberculosis, Gene Analysis (Sequencing)
- IKBKG Testing, LR-PCR & Sanger sequencing
- IKBKG, Ectodermal Dysplasia / Incontinentia Pigmenti, Gene Analysis (Sequencing)
- IKBKG, Ectodermal Dysplasia Incontinentia Pigmenti, Gene Analysis (LR-PCR)
- Inborn Error of Metoblism (IEM) panel 2, Profile test 1. NGS
- Inborn Error of Metoblism (IEM) panel 2, Profile test 1. NGS – Consumable only
- Inborn Error of Metoblism (IEM) panel 2, Profile test 1. NGS – Exclude Consumable
- Inborn Error of Metoblism (IEM) panel 2, Profile tests 1. NGS 2. Sanger Sequencing (Confirmation)
- Inborn Error of Metoblism (IEM) panel 2,Profile test 2. Sanger sequencing (confirmation)
- Inborn Errors of Metabolism (NBS) Panel Phase 1, NBS
- IVD, Isovaleric Acidaemia, Gene Analysis (Sequencing)
- KCNE1, Long QT Syndrome, Gene Analysis (Sequencing)
- KCNE2, Long QT Syndrome, Gene Analysis (Sequencing)
- KCNH2, Long QT Syndrome, Gene Analysis (Sequencing)
- KCNJ1, Bartter Syndrome Type 2, Gene Analysis (Sequencing)
- KCNJ11, Neonatal Diabetes or Hyperinsuliniemic Hypoglycemia of Infancy, Gene Analysis (Sequencing)
- KCNQ1, Long QT Syndrome, Gene Analysis (Sequencing)
- LDLR, Familial Hypercholesterolaemia, Gene Analysis (Sequencing)
- LDLRAP1, Autosomal Recessive Hypercholesterolaemia, Gene Analysis (Sequencing)
- LEPRE1, Osteogenesis Imperfecta Type VIII, Gene Analysis (Sequencing)
- LMNA, Laminopathy / Dilated Cardiomyopathy / Limb Girdle Muscular Dystrophy 1B, Gene Analysis (Sequencing)
- Low-Pass Whole Genome Sequencing (LP-WGS), NGS
- LPG, Lipoprotein glomerulopathy, (PCR & DNA sequencing)
- LPL, Familial dyslipidaemia, (PCR & DNA sequencing)
- LPL, Familial Dyslipidaemia, Gene Analysis (Sequencing)
- m.10158T>C, Mitochondrial Disorders - Leigh Syndrome, Gene Analysis (PCR-RFLP)
- m.10191T>C, Mitochondrial Disorders - Leigh Syndrome, Gene Analysis (PCR-RFLP)
- m.11777C>A, Mitochondrial Disorders - Leigh Syndrome, Gene Analysis (PCR-RFLP)
- m.11778G>A, Mitochondrial Disorders - Leber Hereditary Optic Neuropathy [LHON], Gene Analysis (PCR-RFLP)
- m.12770A>G, Mitochondrial Disorders - MELAS, Gene Analysis (PCR-RFLP)
- m.13045A>C, Mitochondrial Disorders - Leigh Syndrome, Gene Analysis (PCR-RFLP)
- m.13513G>A, Mitochondrial Disorders - MELAS, Gene Analysis (PCR-RFLP)
- m.14459G>A, Mitochondrial Disorders - Leigh Syndrome, Gene Analysis (PCR-RFLP)
- m.14484T>C, Mitochondrial Disorders - Leber Hereditary Optic Neuropathy [LHON], Gene Analysis (PCR-RFLP)
- m.3243A>G, Mitochondrial Disorders - MELAS, Gene Analysis (PCR-RFLP)
- m.3252A>G, Mitochondrial Disorders - MELAS, Gene Analysis (PCR-RFLP)
- m.3271T>C, Mitochondrial Disorders - MELAS, Gene Analysis (PCR-RFLP)
- m.3460G>A, Mitochondrial Disorders - Leber Hereditary Optic Neuropathy [LHON], Gene Analysis (PCR-RFLP)
- m.8344A>G, Mitochondrial Disorders - MERRF, Gene Analysis (PCR-RFLP)
- m.8356T>C, Mitochondrial Disorders - MERRF/MELAS, Gene Analysis (PCR-RFLP)
- m.8993T>C, Mitochondrial Disorders - NARP, Gene Analysis (PCR-RFLP)
- m.8993T>G, Mitochondrial Disorders - NARP, Gene Analysis (PCR-RFLP)
- MCCC1, 3-Methylcrotonyl-CoA Carboxylase Deficiency (Alpha Subunit), Gene Analysis (Sequencing)
- MCCC2, 3-Methylcrotonyl-CoA Carboxylase Deficiency (Beta Subunit), Gene Analysis (Sequencing)
- MECP2, Rett Syndrome, Gene Analysis (MLPA)
- MECP2, Rett Syndrome, Gene Analysis (Sequencing)
- Methylation-Specific Multiplex Ligation-dependent Probe Amplification (MS-MLPA), Single Probemix
- Methylenetetrahydrofolate Reductase Gene C677T Mutation Screening
- MFN2, Charcot-Marie-Tooth Disease, Axonal, Type 2A2, Gene Analysis (Sequencing)
- Microsatellite Markers DNA Identification, per sample pair (PCR) + Molecular Diagnostic Test (Sequencing)
- Mitochondrial 4977-bp Deletion (Kearne Sayre Syndrome / Pearson Syndrome), Gene Analysis (PCR)
- Mitochondrial DNA Large Deletions, Gene Analysis (PCR)
- Mitochondrial DNA NGS
- MLPA, Single Probemix
- MMAA, Methylmalonic Aciduria Type cblA, Gene Analysis (Sequencing)
- MMAB, Methylmalonic Aciduria Type cblB, Gene Analysis (Sequencing)
- MMACHC, Methylmalonic Aciduria and Homocystinuria Type cblC, Gene Analysis (Sequencing)
- MOCS1, Molybdenum Cofactor Deficiency, Gene Analysis (Sequencing)
- MOCS2, Molybdenum Cofactor Deficiency, Gene Analysis (Sequencing)
- MPZ, Charcot-Marie-Tooth Disease1B, 2I, 2J, and 3A, Gene Analysis (Sequencing)
- MTD, Mitochondrial disease, (PCR & DNA sequencing)
- MTHFR, Methylenetetrahydrofolate Reductase Deficiency / Homocystinuria Due to MTHFR Deficiency, Gene Analysis (Sequencing)
- MUT, Methylmalonyl Acidaemia / Methylmalonyl Coenzyme Mutase Deficiency, Gene Analysis (Sequencing)
- MVK, Mevalonae Kinase Deficiency, Gene Analysis (Sequencing)
- MYBPC3, Hypertrophic Cardiomyopathy, Gene Analysis (Sequencing)
- MYH7, Hypertrophic Cardiomyopathy, Gene Analysis (Sequencing)
- MYH9, Thrombocytopenia , Mutation screening
- NAGLU, Mucopolysaccharidosis Type III B, Gene Analysis (Sequencing)
- NBS, Neonatal Bartter syndrome, (PCR & DNA sequencing)
- Neuroblastomas MLPA
- Next Generation Sequencing (NGS) Myeloid Panel
- NGS Panel for Inherited Haematological Diseases
- NICCD1, Neonatal intrahepatic cholestasis caused by citrin deficiency, (PCR & DNA sequencing)
- NICCD2, Neonatal intrahepatic cholestasis due to citrin deficiency a, (PCR & DNA sequencing)
- NIPA1, Hereditary Spastic Paraplegia Type 6, Gene Analysis (Sequencing)
- Non-invasive prenatal testing (NIPT)
- NOTCH3, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy [CADASIL], Gene Analysis (Sequencing)
- NPC1, Niemann-Pick Disease Type C1, Gene Analysis (Sequencing)
- NPC2, Niemann-Pick Disease Type C2, Gene Analysis (Sequencing)
- NPHS1, Nephrotic Syndrome Type 1, Gene Analysis (Sequencing)
- NPHS2, Nephrotic Syndrome Type 2, Gene Analysis (Sequencing)
- NPHS2, Steroid-resistant nephrotic syndrome 1, (PCR & DNA sequencing)
- NR5A1, 46XY Sex Reversal With or Without Adrenal Failure, Gene Analysis (Sequencing)
- OI panel cost (Profile)
- Osteogenesis Imperfecta (OI) panel - Profile test 1: Next Generation Sequencing, NGS (Profile)
- OTC, Ornithine Transcarbamylase Deficiency, Gene Analysis (Sequencing)
- PABPN1, Oculopharyngeal muscular dystrophy, Gene Analysis (PCR)
- PABPN1, Oculopharyngeal Muscular Dystrophy, Gene analysis (Sequencing)
- PANK2, Pantothenate Kinase-associated Neurodegeneration / Hallervorden-Spatz Syndrome, Gene Analysis (Sequencing)
- PARK2, Parkinson Disease, Gene Analysis (Sequencing)
- Parkinson Disease, Gene Analysis (MLPA)
- PC, Pyruvate Carboxylase Deficiency, Gene Analysis (Sequencing)
- PCCA, Propionic acidaemia, (PCR & DNA sequencing)
- PCCA, Propionic Acidemia, Gene Analysis (Sequencing)
- PCCB, Propionic acidaemia, (PCR & DNA sequencing)
- PCCB, Propionic Acidemia, Gene Analysis (Sequencing)
- PDHA1, Pyruvate Dehydrogenase Deficiency, Gene Analysis (Sequencing)
- PEX1, Peroxisome Biogenesis Disorders (Zellweger Syndrome / Neonatal Adrenoleucodystrophy / Infantile Refsum Syndrome), Gene Analysis (Sequencing)
- PHEX, X-Linked Hypophosphataemic Rickets, Gene Analysis (Sequencing)
- PHKA2, Glycogen Storage Disease Type IXa, Gene Analysis (Sequencing)
- PINK1, Parkinson Disease 6, Gene Analysis (Sequencing)
- PKD1 NGS
- PKP2, Arrhythmogenic Right Ventricular Dysplasia / Plakophilin 2, Gene Analysis (Sequencing)
- PMM2, Congenital Disorder of Glycosylation Type 1A, Gene Analysis (Sequencing)
- PMP22, Charcot-Marie-Tooth Disease 1A / Hereditary Neuropathy with Liability to Pressure Palsies , Gene Analysis (MLPA)
- PMP22, Charcot-Marie-Tooth Disease 1A and 1E / Dejerine-Sottas Syndrome, Gene Analysis (Sequencing)
- PNKD, Paroxysmal Nonkinesiogenic Dyskinesia, Gene Analysis (Sequencing)
- POD, P450 oxidoreductase deficiency, (PCR & DNA sequencing)
- POLG, mtDNA Polymerase Gamma Disease, Gene Analysis (Sequencing)
- POR, Cytochrome P450 Oxidoreductase Deficiency, Gene Analysis (Sequencing)
- POU1F1, Combined Pituitary Hormone Deficiency Type 1, Gene Analysis (Sequencing)
- PPIB, Osteogenesis Imperfecta Type IX, Gene Analysis (Sequencing)
- PPOX, Variegate Porphyria, Gene Analysis (Sequencing)
- PPP2R2B, Spinocerebellar Ataxia 12, Gene Analysis (PCR)
- PPT1, Infantile Neuronal Ceroid Lipofuscinoses / CLN1, Gene Analysis (Sequencing)
- PRKAR1A, Carney Complex, Gene Analysis (Sequencing)
- PRKCG, Spinocerebellar Ataxia 14, Gene Analysis (Sequencing)
- PROP1, Combined Pituitary Hormone Deficiency Type 2, Gene Analysis (Sequencing)
- Prothrombin G20210A Mutation Screening
- PTPN11, Noonan Syndrome/Leopard Syndrome, Gene Analysis (Sequencing)
- PTS, Hyperphenylalaninaemia Due to 6-Pyruvoyltetrahydropterin Synthase Deficiency, Gene Analysis (Sequencing)
- PYGL, Glycogen storage disease type VI, (PCR & DNA sequencing)
- PYGL, Glycogen Storage Disease Type VI, Gene Analysis (Sequencing)
- QT1, Long QT syndrome type 1, (PCR & DNA sequencing)
- QT2, Long QT syndrome type 2, (PCR & DNA sequencing)
- QT3, Long QT syndrome type 3, (PCR & DNA sequencing)
- QT5, Long QT syndrome type 5, (PCR & DNA sequencing)
- QT6, Long QT syndrome type 6, (PCR & DNA sequencing)
- Renal panel cost (Profile)
- Renal Panel- Profile test 1: Next Generation Sequencing, NGS (Profile)
- RPS19, Diamond-Blackfan Anaemia Type 1, Gene Analysis (Sequencing)
- RyR2, First Tier Screening (16 Selected Exons) for Catecholaminergic Polymorphic Ventricular Tachycardia Type 1, Gene Analysis (Sequencing)
- RyR2, Second Tier Screening (13 Selected Exons) for Catecholaminergic Polymorphic Ventricular Tachycardia Type 1, Gene Analysis (Sequencing)
- RyR2, Third Tier Screening (16 Selected Exons) for Catecholaminergic Polymorphic Ventricular Tachycardia Type 1, Gene Analysis (Sequencing)
- SBD, Shwachman-Diamond syndrome, (PCR & DNA sequencing)
- SCN1A, Severe Myoclonic Epilepsy of Infancy / Dravet Syndrome, Gene Analysis (Sequencing)
- SCN5A, Long QT Syndrome 3 / Brugada Syndrome / Familial Sick Sinus Syndrome, Gene Analysis (Sequencing)
- SCNN1B, Liddle Syndrome, Gene Analysis (Sequencing)
- SCNN1G, Liddle Syndrome, Gene Analysis (Sequencing)
- SCNNIB, Liddle's syndrome, (PCR & DNA sequencing)
- SDHB, Hereditary Paraganglioma-Pheochromocytoma Syndromes, Gene Analysis (Sequencing)
- SDHC, Hereditary Paraganglioma-Pheochromocytoma Syndromes, Gene Analysis (Sequencing)
- SDHD, Hereditary Paraganglioma-Pheochromocytoma Syndromes, Gene Analysis (Sequencing)
- SERPINA1, Alpha-1 Antitrypsin Deficiency, Gene Analysis (Sequencing)
- SF1, 46,XY Disorders of Sex Development, Gene Analysis (Sequencing)
- SGSH, Mucopolysaccharidosis Type III A, Gene Analysis (Sequencing)
- SH2D1A, X-linked Lymphoproliferative Syndrome, Gene Analysis (Sequencing)
- SLC12A1, Bartter Syndrome Type 2, Gene Analysis (Sequencing)
- SLC12A3, Gitelman Syndrome, Gene Analysis (Sequencing)
- SLC22A5, Primary Carnitine Deficiency, Gene Analysis (Sequencing)
- SLC25A13, Citrin Deficiency / Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency , Gene Analysis (Sequencing)
- SLC25A15, Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome, Gene Analysis (Sequencing)
- SLC25A20, Carnitine-Acylcarnitine Translocase Deficiency, Gene Analysis (Sequencing)
- SLC25A4, Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions 3 , Gene Analysis (Sequencing)
- SLC2A1, Blood-Brain Barrier Glucose Transport Defect, Gene Analysis (Sequencing)
- SLC37A4, Glycogen Storage Disease Type Ib, Gene Analysis (Sequencing)
- SLC3A1, Cystinuria Type A, Gene Analysis (Sequencing)
- SLC4A1, Distal Renal Tubular Acidosis, Gene Analysis (Sequencing)
- SLC6A8, X-linked Creatine Deficiency Syndrome, Gene Analysis (Sequencing)
- SLC7A9, Cystinuria Type B, Gene Analysis (Sequencing)
- SMN1, Spinal Muscular Atrophy & Carrier Testing, Gene Analysis (MLPA)
- SMN1, Spinal Muscular Atrophy, Gene Analysis (PCR-RFLP)
- SMPD1, Niemann-Pick Disease Types A & B, (PCR & DNA sequencing)
- SMPD1, Niemann-Pick Disease Types A and B, Gene Analysis (Sequencing)
- SPAST, Hereditary Spastic Paraplegia 4, Gene Analysis (Sequencing)
- SPAST, Hereditary spastic paraplegia, (PCR & DNA sequencing)
- SPG11, Hereditary Spastic Paraplegia 11, Gene Analysis (Sequencing)
- SPG3A, Hereditary Spastic Paraplegia 3, Gene Analysis (Sequencing)
- SPG3A, Hereditary spastic paraplegia, (PCR & DNA sequencing)
- SPG6, Hereditary Spastic Paraplegia 6, Gene Analysis (Sequencing)
- SPG7, Hereditary Spastic Paraplegia 7, Gene Analysis (Sequencing)
- SRD, 5-alpha reductase 2 deficiency, (PCR & DNA sequencing)
- SRD5A2, 5-Alpha Reductase-2 Deficiency, Gene Analysis (Sequencing)
- STAR, Lipoid Congenital Adrenal Hyperplasia, Gene Analysis (Sequencing)
- SUOX, Sulphite Oxidase Deficiency, Gene Analysis (Sequencing)
- SURF1, Cytochrome c Oxidase Deficiency / Leigh Syndrome, Gene Analysis (Sequencing)
- TALDO1, Transaldolase 1 Deficiency, Gene Analysis (Sequencing)
- TAZ, Barth Syndrome / Dilated Cardiomyopathy / Left Ventricular Non-compaction, Gene Analysis (Sequencing)
- TBP, Spinocerebellar Ataxia 17, Gene Analysis (PCR)
- TH, Tyrosine Hydroxylase Deficiency, Gene Analysis (Sequencing)
- THRB, Resistance to thyroid hormone, (PCR & DNA sequencing)
- THRB, Resistance to Thyroid Hormone, Gene Analysis (Sequencing)
- TINF2, Dyskeratosis Congenita, Gene Analysis (Sequencing)
- TOR1A, Autosomal dominant dystonia 1, (PCR & DNA sequencing)
- TOR1A, Early-Onset Primary Torsion Dystonia / DYT1 c.907_909delGAG, Gene Analysis (Sequencing)
- TPMT, TPMT genotyping, (PCR & DNA sequencing)
- TPP1, Neuronal Ceroid Lipofuscinoses / CLN2, Gene Analysis (Sequencing)
- Transferrin Isoforms
- TTR, Familial Transthyretin Amyloidosis, Gene Analysis (Sequencing)
- TYMP, Mitochondrial neurogastrointestinal encephalopathy syndrome, (PCR & DNA sequencing)
- UGT1A1*28, Pharmacogenetic Test for Irinotecan, Gene Analysis (Sequencing)
- UGT1A1, Gilbert Syndrome / Criggler-Najjar Syndrome, Gene Analysis (Sequencing)
- UMPS, Orotic Aciduria Type 1, Gene Analysis (Sequencing)
- UPB1, Beta-ureidopropionase Deficiency, Gene Analysis (Sequencing)
- VHL, von Hippel Lindau Syndrome, Gene Analysis (MLPA)
- VHL, von Hippel Lindau Syndrome, Gene Analysis (Sequencing)
- Whole Exome Sequencing - Profile test 1: Next Generation Sequencing, NGS (Profile)
- Whole Exome Sequencing - Profile test 1-1: Next Generation Sequencing, NGS (except consumables) (Profile)
- Whole Exome Sequencing - Profile test 1-2: Next Generation Sequencing, NGS (consumables) (Profile)
- Whole Exome Sequencing - Profile test 2.: Sanger Sequencing (NGS confirmation) (Profile)
- Whole Exome Sequencing, Profile tests: 1. NGS 2. Sanger Sequencing (NGS confirmation) (Profile)
- Williams-Beuren Syndrome, Gene Analysis (MLPA)
- X-inactivation, Gene Analysis (PCR)
- Atypical Mycobacteria (Sequencing)
- Atypical Mycobacteria, Tissue (PCR)
- Bacteria Detection in Specimen (PCR)
- Bacteria Detection in Specimen (Sequencing)
- Bacterial Identification (Sequencing)
- Bordetella pararpertussis DNA (PCR)
- Bordetella pertussis DNA (PCR)
- Chlamydia pneumoniae DNA (PCR)
- Chlamydia trachomatis DNA (PCR)
- Clostridium difficile Toxin B Gene DNA
- Cytomegalovirus DNA (PCR)
- Dengue Virus Type 3 RNA (PCR)
- Diarrhoeal Viruses (PCR)
- Enterovirus RNA (PCR)
- Epstein-Barr Virus [EBV] Detection (qPCR)
- Epstein-Barr Virus DNA (PCR)
- Epstein-Barr Virus EBER RNA Detection (ISH)
- Fungal Identification (Sequencing)
- Hepatitis B Virus DNA Quantiation (qPCR)
- Hepatitis C Virus (PCR)
- Hepatitis C Virus Genotyping
- Hepatitis C Virus RNA Quantiation (qPCR)
- Herpes Simplex Virus DNA (PCR)
- Herpes Simplex Virus Type 1 DNA (PCR)
- Herpes Simplex Virus Type 2 DNA (PCR)
- Human Herpes Virus Type 6 [HHV6] Detection (PCR)
- Human Herpes Virus Type 7 [HHV7] Detection (PCR)
- Human Herpes Virus Type 8 [HHV8] Detection (PCR)
- Human Immunodeficiency Virus RNA Quantitation (qPCR)
- Human Metapneumovirus RNA (PCR)
- Human Papillomavirus [HPV] Detection (Digene Test)
- Human Papillomavirus [HPV] Detection (ISH)
- Human Papillomavirus [HPV] Detection (PCR and Typing)
- Human Papillomavirus [HPV] Genotyping
- Human Papillomavirus Screening for Types 6, 11, 16, 18, 31 and 33 (PCR)
- Influenza A Virus RNA (PCR)
- Influenza A Virus Subtype H1 RNA - Swine (PCR)
- Influenza A Virus Subtype H1 RNA (PCR)
- Influenza A Virus Subtype H3 RNA (PCR)
- Influenza A Virus Subtype H5 RNA (PCR)
- Influenza A Virus Subtype H7 RNA (RT-PCR)
- Influenza A Virus Subtype H9 RNA (PCR)
- Legionella pneumophila DNA (PCR)
- Methicillin-Resistant Staphylococcus aureus DNA (PCR)
- Middle East Respiratory Syndrome Coronavirus (MERS-CoV) PCR
- Mycobacterium leprae (PCR)
- Mycobacterium tuberculosis - IS6110 and mtp40 (PCR)
- Mycobacterium tuberculosis Detection (PCR)
- Mycobacterium tuberculosis Detection (qPCR)
- Mycobacterium tuberculosis Drug Resistance (PCR-SSCP)
- Mycobacterium tuberculosis Drug Resistance (Sequencing)
- Mycobacterium tuberculosis Identification (Sequencing)
- Mycobacterium tuberculosis RNA (AMTDT)
- Mycoplasma pneumoniae DNA (PCR)
- Neisseria gonorrhoae DNA (PCR)
- Norovirus RNA (PCR)
- Parvovirus B19 DNA (PCR)
- PCR for Meningitis/Encephalitis (ME) Panel (except consumables)
- PCR for Meningitis/Encephalitis (ME) Panel (include consumables only)
- PCR for Meningitis/Encephalitis (ME) Panel (Profile)
- PCR for Respiratory Panel
- Polyoma BK Virus, Body Fluid (PCR)
- Polyoma BK Virus, Tissue (PCR)
- Polyoma JC Virus, Body Fluid (PCR)
- Polyoma JC Virus, Tissue (PCR)
- Polyomavirus DNA (PCR)
- Rotavirus RNA (PCR)
- SARS Coronavirus (PCR)
- Varicella Zoster Virus DNA (PCR)
- Virus Detection in Specimen (PCR)
- Virus Detection in Specimen (Sequencing)
- Whipples Disease,Tropheryma whippelii Detection (PCR)
- B Cell Function Tests (Profile)
- Antibody Screening - Class I
- Antibody Screening - Class I and II
- Antibody Screening - Class I and II + Final CDCXM for Patient's Sera vs 1st Donor Cells
- Antibody Screening - Class I and II + HLA Typing - HLA-A, B and DRB1, Low Resolution
- Antibody Screening - Class II
- Antibody Screening - PRA for Class I only
- B Cell Function - IgA
- B Cell Function - IgG
- B Cell Function - IgM
- Donor-Recipient Crossmatch for Related Renal Transplantation - CDCXM for Patient's Sera vs 1st Donor Cells with DTT Treatment
- Donor-Recipient Crossmatch for Related Renal Transplantation - CDCXM for Patient's Sera vs Subsequent Donor Cells with DTT Treatment
- Donor-Recipient Crossmatch for Related Renal Transplantation - Final CDCXM for Patient's Sera vs 1st Donor Cells
- Donor-Recipient Crossmatch for Related Renal Transplantation - Final CDCXM for Patient's Sera vs Subsequent Donor Cells
- Donor-Recipient Crossmatch for Related Renal Transplantation - Preliminary CDCXM for Patient's Sera vs Subsequent Donor Cells
- Engraftment Testing, Post-Transplant
- Engraftment Testing, Pre-Transplant
- HLA Typing - CT for Unrelated BMT Donor or Recipient (HLA-A, B, C and DRB1, High Resolution)
- HLA Typing - HLA Class I ( HLA-A, B and C, Low Resolution)
- HLA Typing - HLA Class I ( HLA-A, B, Low Resolution)
- HLA Typing - HLA-A, B and DRB1, Low Resolution
- HLA Typing - HLA-A, B and DRB1, Low Resolution + Preliminary CDCXM for Patient's Sera vs 1st Donor Cells + Antibody Screening - Class I and II
- HLA Typing - HLA-A, B and DRB1, Low Resolution + Processing of Cadaveric Kidney Donor
- HLA Typing - HLA-A, B LR and DRB1, High Resolution
- HLA Typing - HLA-A, B, C and DRB1, Low Resolution
- HLA Typing - HLA-A, B, C, DRB1 and DQB1, High Resolution
- HLA Typing - HLA-A, High Resolution
- HLA Typing - HLA-A, Low Resolution
- HLA Typing - HLA-B, High Resolution
- HLA Typing - HLA-B, Low Resolution
- HLA Typing - HLA-B27, Low Resolution
- HLA Typing - HLA-C, High Resolution
- HLA Typing - HLA-C, Low Resolution
- HLA Typing - HLA-DQB1, High Resolution
- HLA Typing - HLA-DQB1, Low Resolution
- HLA Typing - HLA-DRB1, High Resolution
- HLA Typing - HLA-DRB1, Low Resolution
- HLA Typing - Routine HLA-B*1502
- HLA Typing - Routine HLA-B*5701
- HLA Typing - Routine HLA-B*5801
- HLA Typing - Urgent HLA-B*1502
- HLA Typing - Urgent HLA-B*5701
- HLA Typing - Urgent HLA-B*5801
- HLA Typing, High Resolution
- HLA Typing, Low Resolution
- KIR typing
- NK Cell Function - Cytotoxicity (IL-2 Stimulation)
- NK Cell Function - Cytotoxicity (Resting Stage + IL-2 Stimulation) (Profile)
- NK Cell Function - Cytotoxicity (Resting Stage)
- NK Cell Function - Degranulation, Granzyme, Perforin
- NK Cell Function Tests (Profile)
- Preliminary CDCXM for Patient's Sera vs 1st Donor Cells
- Processing of Cadaveric Kidney Donor
- Quantitative Assay for TREC & KREC
- TPMT + NUDT-15 Genotyping
- DCLRE1C (Artemis) (for family member), Omenn syndrome, Severe combined immunodeficiency, Gene Analysis (Sequencing)
- 27-Hydroxycholesteral, Free
- 27-Hydroxycholesteral, Total
- 5-Flourouracil
- ADAMTS13 Activity
- ADAMTS13 Assay
- Anti-IFN Gamma Neutralizing Antibody by Flow Cytometry
- Anti-Interferon gamma Antibodies ELISA
- Biopsy, Complex
- Bone Marrow Morphology Analysis
- BTK (for family member), X-linked agammaglobulinemia (XLA) / Predominately antibody deficiencies, Gene Analysis (Sequencing)
- BTK, X-linked agammaglobulinemia (XLA) / Predominately antibody deficiencies, Gene Analysis (Sequencing)
- CAR-T cells enumeration
- CD40L (for family member), Hyper IgM Syndrome, Gene Analysis (Sequencing)
- CD40L, Hyper IgM Syndrome, Gene Analysis (Sequencing)
- Coenzyme Q10, Total (TQ10)
- Collagen binding
- CYBA, (for family member) Chronic granulomatous disease: autosomal, Gene Analysis (Sequencing)
- CYBA, Chronic granulomatous disease: autosomal, Gene Analysis (Sequencing)
- CYBB (for family member), X-linked Chronic Granulomatous Disease (CGD), Gene Analysis (Sequencing)
- CYBB, X-linked Chronic Granulomatous Disease (CGD), Gene Analysis (Sequencing)
- CYP2C19*17 genotyping
- CYP2C19*2/*3 genotyping
- CYP2C19*2/*3/*17 genotyping
- DCLRE1C (Artemis), Omenn syndrome, Severe combined immunodeficiency, Gene Analysis (Sequencing)
- Eculizumab, serum
- Edoxaban Assay
- ELANE (ELA2) (for family member), Congenital ELANE-related Neutropenia, Gene Analysis (Sequencing)
- ELANE (ELA2), Congenital ELANE-related Neutropenia, Gene Analysis (Sequencing)
- Enumeration of Chimeric Antigen Receptor T-cells (CAR-T)
- Factor XIII assay (ammonia release assay)
- FAMS, Family genetic study, (PCR & DNA sequencing)
- Female Androgen Profile (Profile)
- First engraftment study
- Flow Cytometry for platelet markers (CD41, CD42b, CD61)
- Fluorescence In-situ Hybridisation [FISH] - Interphase
- Fluorescence In-situ Hybridisation [FISH] - Interphase, per Hybridisation
- Fluorescence In-situ Hybridisation [FISH] - Metaphase, per Hybridisation
- Haemoglobin Study
- HLA Typing - HLA-DRB1, Low Resolution and DRB1, High Resolution
- HLA typing, High Resolution (NGS)
- HLA typing, High Resolution, multi-pattern (NGS),Urine/Biopsy/Blood
- HNA Antibody test (Profile)
- HNA genotyping
- HNA-1-4a,5 Antibody test (Profile)
- HNA-4b Antibody test (Profile)
- IL12RB1 (CD212), (for family member) Mendelian susceptibility to mycobacterial disease (MSMD), Gene Analysis (Sequencing)
- IL12RB1 (CD212), Mendelian susceptibility to mycobacterial disease (MSMD), Gene Analysis (Sequencing)
- IL2RG (for family member), X-linked Combined immunodeficiency (SCID) / T-B+SCID, Gene Analysis (Sequencing)
- IL2RG, X-linked Combined immunodeficiency (SCID) / T-B+SCID, Gene Analysis (Sequencing)
- Immune cell function test
- Immunophenotyping (Leukaemia)
- ITGB2 (CD18/LAD1) (for family member), Leukocyte adhesion deficiency, Gene Analysis (Sequencing)
- ITGB2 (CD18/LAD1), Leukocyte adhesion deficiency, Gene Analysis (Sequencing)
- Lymphocyte Transformation Test
- Measurable Residual Disease (MRD) by Flow Cytometry
- Microsatellite Markers DNA Identification, per sample pair (PCR)
- Molecular Diagnostic Test (PCR)
- Molecular Diagnostic Test (Sequencing)
- MRD (ALL) monitoring by Flow cytometry for T-ALL - consumables
- MRD (ALL) monitoring by Flow cytometry for T-ALL - without consumables
- MRD (AML) monitoring by Flow cytometry - consumables
- MRD (AML) monitoring by Flow cytometry - without consumables
- MRD (B-ALL) monitoring by Flow cytometry - consumables
- MRD (B-ALL) monitoring by Flow cytometry - exclude consumables
- Nucleic Acid Detection, on Liquid-base Specimen (Hybridization)
- Nucleic Acid Detection, on Slide (Hybridization)
- Plasma Porphyrin Fluorescence Scanning
- Platelet Aggregation Test
- Platelet antibody by antigen capture by ELISA method
- Platelet Antibody by Luminex
- Quantitative Fluorescent Polymerase Chain Reaction [QF-PCR]
- RAG1 (for family member),Combined immunodeficiency (SCID) / T-B-SCID, Gene Analysis (Sequencing)
- RAG1, Combined immunodeficiency (SCID) / T-B-SCID, Gene Analysis (Sequencing)
- RAG2 (for family member), Combined cellular and humoral immune defects with granulomas, Gene Analysis (Sequencing)
- RAG2, Combined cellular and humoral immune defects with granulomas, Gene Analysis (Sequencing)
- RBC Membrane Protein Analysis - consumables
- RBC Membrane Protein Analysis - without consumables
- RBC Pyruvate Kinase Enzyme Assay
- Ristocetin-induced platelet agglutination (RIPA)
- Rivaroxaban assay
- SCT (Cell selection) - Component test 1
- SCT (Cell selection) - Component test 2
- SCT (Cell selection) - Profile test
- SCT (Cryopreservation)
- SCT (DLH)
- SCT (HAV1)
- SCT (HAV2)
- SCT (Thaw and Dilute)
- serum Copeptin
- SH2D1A (for family member), X-linked Lymphoproliferative Disease (XLP), Gene Analysis (Sequencing)
- SH2D1A, X-linked Lymphoproliferative Disease (XLP), Gene Analysis (Sequencing)
- STAT1 (for family member), MSMD / CMC Autosomal Dominant Chronic Mucocutaneous Candidiasis, Gene Analysis (Sequencing)
- STAT1, MSMD / CMC Autosomal Dominant Chronic Mucocutaneous Candidiasis, Gene Analysis (Sequencing)
- STAT3 (for family member), Hyper-IgE recurrent infection syndrome, Autoimmune disease, Gene Analysis (Sequencing)
- STAT3, Hyper-IgE recurrent infection syndrome, Autoimmune disease, Gene Analysis (Sequencing)
- Subsequent engraftment study
- Targeted Screening for One Mutation (Sequencing)
- Targeted Screening for Two Mutations (Sequencing)
- Uracil, plasma
- Voriconazole
- vWF F8 Binding - consumables
- vWF F8 Binding - without consumables
- vWF-Activity
- vWF-Multimeric analysis
- WAS (for family member), Wiskott–Aldrich syndrome, Severe congenital neutropenia, Gene Analysis (Sequencing)
- WAS, Wiskott–Aldrich syndrome, Severe congenital neutropenia, Gene Analysis (Sequencing)
- XIAP (BIRC4) (for family member) , Lymphoproliferative syndrome, Gene Analysis (Sequencing)
- XIAP (BIRC4) , Lymphoproliferative syndrome, Gene Analysis (Sequencing)
Note: 1. The Consultant Pathologists may refuse any sample that is considered not suitable for examination. 2. Samples submitted for examination will remain the property of the Hospital Authority and may be disposed of in any way considered suitable by the Consultant Pathologists. 3. The above charges include the issue of one copy of examination report. 1. 病理科顧問醫生有權拒絕化驗任何不適合的樣本。 2. 凡供化驗的樣本， 均屬醫院管理局所有，並可由病理科顧問醫生決定處置的方法。3. 以上費用包括簽發檢驗報告一份。