- Biopsy, Bone Marrow, Trephine and Clot
- Biopsy, Complex
- 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)
- 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
- Adalimumab, serum
- 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
- Anti-adalimumab, serum
- Anticonvulsant Profile
- Anti-infliximab
- 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
- Infliximab, 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]
- Lyso-sphingomyelin (Lyso-SM), plasma
- 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
- Mexiletine, serum
- Mycophenolic acid
- Newborn Screening Panel, Dried Blood Spot
- 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 Globotriaosylsphingosine (lyso-Gb3)
- 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
- 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 Dexamethasone
- 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
- Thiopurine metabolites
- 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 B
- 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
- S-sulfocysteine, plasma
- 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
- 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', 30', 60', 90', 120', 150'}
- 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] - {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 - {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 - {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 - {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', 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, GH, GLU x 0', 15', 20', 30', 45', 60', 90', 120'}
- Insulin Tolerance Test [ITT] - {CORT, GH, GLU x 0', 30', 45', 60', 90', 120'}
- 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 [LDSSYN] - {CORT x 0', 30'}
- 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'}
- Synacthen Test [LDSSYN] - {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
- Antimony, Urine, Spot
- 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
- Chromium, Urine, Spot
- Chyle, Urine
- Citric acid, urine, spot
- Cobalt cr Ratio, Urine, Spot
- Cobalt, Urine, Spot
- 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
- Nickel, Urine, Spot
- 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
- Thallium, Urine, Spot
- 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
- 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
- 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
- Autohaemolysis Test
- Beta globin genotype
- 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
- 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)
- ALL Minimal Residual Disease (MRD) marker identification (NGS)
- ALL Minimal Residual Disease (MRD) marker identification (qPCR & Equipment)
- 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
- 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
- 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)
- 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
- Translocation Detection in Solid Tumour (PCR)
- TruSight Oncology 500
- 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 (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
- Cardiac Panel- Profile test 1: Next Generation Sequencing, NGS
- 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
- EIEE panel cost
- 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 gene panel for IEI
- 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
- Osteogenesis Imperfecta (OI) panel - Profile test 1: Next Generation Sequencing, NGS
- 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
- Renal Panel- Profile test 1: Next Generation Sequencing, NGS
- 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
- Whole Exome Sequencing - Profile test 2.: Sanger Sequencing (NGS confirmation)
- Whole Exome Sequencing, Profile tests: 1. NGS 2. Sanger Sequencing (NGS confirmation)
- 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
- 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)
- 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
- B Cell Function Tests
- 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 Low Resolution 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)
- NK Cell Function - Cytotoxicity (Resting Stage)
- NK Cell Function - Degranulation, Granzyme, Perforin
- NK Cell Function Tests
- Preliminary CDCXM for Patient's Sera vs 1st Donor Cells
- Processing of Cadaveric Kidney Donor
- Quantitative Assay for TREC & KREC
- TPMT + NUDT-15 Genotyping
- 27-Hydroxycholesteral, Free
- 27-Hydroxycholesteral, Total
- 5-Flourouracil
- ADAMTS13 Activity
- ADAMTS13 Assay
- Allergy Xplorer ALEX
- Anti-IFN Gamma Neutralizing Antibody by Flow Cytometry
- Anti-Interferon gamma Antibodies ELISA
- Anti-MAG antibodies
- Apixaban Assay
- 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)
- Chemical Pathology Consultation test
- Coenzyme Q10, Total (TQ10)
- Collagen binding
- CSF blast detection by flow cytometry
- 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
- Dabigatran Assay
- DCLRE1C (Artemis) (for family member), Omenn syndrome, Severe combined immunodeficiency, Gene Analysis (Sequencing)
- 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 VIII assay (Chromogenic)
- Factor XIII assay (ammonia release assay)
- FAMS, Family genetic study, (PCR & DNA sequencing)
- Female Androgen 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
- HNA genotyping
- HNA-1-4a,5 Antibody test
- HNA-4b Antibody test
- 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
- MRD (AML) monitoring by Flow cytometry
- MRD (B-ALL) monitoring by Flow cytometry
- 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
- 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
- T Cell subset enumeration
- Targeted Screening for One Mutation (Sequencing)
- Targeted Screening for Two Mutations (Sequencing)
- Uracil, plasma
- Voriconazole
- vWF F8 Binding
- 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)
注：1. 病理科顾问医生有权拒绝化验任何不适合的样本。 2. 凡供化验的样本， 均属医院管理局所有，并可由病理科顾问医生决定处置的方法。 3. 以上费用包括签发检验报告一份。