Lab Tests

Showing 101–200 of 905 results

Muscular Dystrophy Gene Panel

MPZ Full Length Gene Sequence Analysis (Charcot-Maria-Tooth Disease)

MPN – Molecular Panel ( 4 markers )

MLL t(4;11)(q21;q23) Qualitative

MLC1 Gene Mutation Analysis (Agrawal Mutation)

Microsatellite Instability (Lynch Syndrome/ Colorectal Cancer)

Microcephaly Gene Panel

Microarray (60K) Blood

MGMT Methylation Assay

Methylenetetrahydrofolate Reductase (MTHFR), FACTOR V (F5), FACTOR II (F2)

Methylenetetrahydrofolate Reductase (MTHFR – 2 Variants C677T, A1298C)

Metabolic Disorder Gene Panel

Melanoma/Skin Tumors

MECP2 Full Gene Mutation Analysis (RETT Syndrome)

Maturity-Onset Diabetes of the Young (MODY) Gene Panel

Lysosomal Storage Disorder Gene Panel

Lung & Colon Cancer Gene Panel

Leigh Syndrome & Mitochondrial Encephalopathy Gene Panel

KRAS Mutation Screening (Codons 12 & 13)

JAK2 Gene, V617F Mutation Detection

Jak 2 Mutation Detection Panel (Exons 12-15)

Irnotecan Toxicity Assessment(UGT1A1 Genotyping)

Inborn Error Of Metabolism (Urine) by GCMS

Inborn Error Of Metabolism (DBS)

Huntington Disease (HD mutation screening)

Human Papilloma Virus (HPV High-Risk) PCR with Genotyping

Human Inmmuno-defecincy Virus – 1 (HIV-1) Drug Resistance Genotype

Human Immunodeficiency Virus 1 (HIV- 1) Quantitative PCR

Human Immunodeficiency Virus 1 (HIV- 1) Qualitative PCR

HR-HLA A, B, DRB1

HR-HLA A, B, C, DRB1, DQB1

HLA-DRB1*1501 Genotyping (Multiple Sclerosis)

HLA-B*57:01 Genotyping (for Abacavir Hypersensitivity)

HLA A, B, DRB1-Low resolution

HLA A, B, C, DRB1, DQB1 (Any One)-Low resolution

HLA A, B, C, DRB1, DQB1- Low resolution

HIV-1 Proviral DNA PCR

Herpes Simplex Virus Type 1 & Type 2 (HSV 1 & 2) Qualitative PCR

Hereditary Spastic Paraplegia Gene Panel

Hepatitis C Virus (HCV) Genotype

Hepatitis B Virus (HBV) Genotype

Hemophilia A Common Mutation Screening (Factor VIII Intron 22 and Intron 1 Inversion analysis)

Hemochromatosis HFE Full Gene Sequence Analysis

Hemochromatosis Common Mutation Analaysis in HFE Gene (H63D, S61C & C282Y)

HbE (Hemoglobin E) mutation screening

HBB Full Gene Analysis (?-Thallassemia)

Haemophilia A & B gene Panel

Gynaecological cancer Gene Panel

Glycogen Storage Disorder Gene Panel

Glucose-6-Phosphate Dehydrogenase (G6PD) full length gene sequence analysis

Gilbert Syndrome (UGT1A1 Genotyping)

GATA2 Full length gene sequencing (Chronic Neutropenia, MonoMac Syndrome, Mylodysplasia, AML)

Gastro-Intestinal Cancer Gene Panel

Fragile X Syndrome (FMR1)

FLT3/ITD Allelic Ratio

FLT3 (ITD, D835Y) MUTATION

Familial Mediterranean Fever: MEFV full gene Analysis

FACTOR V Leiden Mutation Screening (F5 – G1691A)

FACTOR II Mutation Screening (F2 – G20210A)

Epidermal Growth Factor Receptor Mutation Analysis (EGFR – Exon 18, 19, 20, 21)

Endocrine Cancer Gene Panel

Ebstein Barr Virus Qualitative PCR

Early Infantile Epileptic Encephalopathy Gene Panel

E2A t(1;19)(q23;p13) Qualitative PCR

Dystonia Gene Panel

Duchenne/Becker Muscular Dystrophy mutation screening (DMD – 26 exons)

DMD (79 Exons)/DMD Carrier Screening

Deafness Gene Panel

Cytomegalovirus (CMV) Quantitative PCR

Cytomegalo Virus (CMV), Qualititative ,PCR

Cytochrome P450 2D6 Genotyping (CYP2D6 – Alleles)

Cytochrome P450 2C19 Genotyping (CYP2C19) Clopidogrel resistance (2,3,4,10)

Cystic Fibrosis: CFTR full gene sequence analysis

Cystic Fibrosis mutation screening (CFTR – Del 508 )

Cystic Fibrosis Mutation Screening (CFTR – del 508, G551D/R553X, G542X)

Congenital Myopathy Gene Panel

Congenital Adrenal Hyperplasia (CAH full gene sequence analysis)

Complete Inherited Disease Panel

Common Neurological/neuromuscular diseases Gene Panel

cKIT Mutation Screening (Exons 9, 11, 13, 17) AML/Gastrointestinal Stromal Tumors

Chronic Leukemia (CNL)(CSF3R gene – exon 14 & 17; SETBP gene – exon 4)

CHLAMYDIA TRACHOMATIS,PCR(QUALITIATIVE)

Chikungunya RNA Detection by PCR/Blood

CEBPA Full Gene Mutation Analysis

CBFB-MYH11 inv(16) Qualitative

Cardiomyopathy Gene Panel

Cardiac Channelopathy Gene Panel

Cancer Syndrome Gene Panel

Cancer Hot Spot Gene Panel

CALR Mutation Analysis (Deletion or Insertion in Exon 9)

Breast Cancer Gene panel

Breast and Ovarian Cancer Gene Panel

BRCA 1 & 2 Gene Panel

BRAF Mutation Analysis (V600E)

BK/JC Qualitative PCR

Beta Thalassemia Single [9 Mutations]

Beta Thalassemia Single [12 Mutations]

Beta Thalassemia Couple [9 Common Mutations]

Benign Infantile Epilepsy Gene Panel

BCR-ABL1 Quantitative PCR with IS Scale**