A
- Achondroplasia (FGFR3 full gene sequencing)
- Achondroplasia (FGFR3 gene G1138A, G1138C)
- ALK/EML4 (NSCLC) – FISH
- ALL cyto panel (karyo+FISH)
- ALL PCR panel (BCR/ABL, TEL/AML1, MLL, E2A)
- Allogrove Syndrome (AAAS Full Gene Sequence Analysis)
- Alzheimer Disease (Apo E3/E4)
- AML Cyto Panel (karyo+FISH)
- AML Panel (Myeloid NGS Panel + AML FISH Panel + Karyotyping)
- AML PCR Panel (AML/ETO, inv(16), PML/RARA)
- AML Prognostic PCR panel (AML/ETO, inv(16), PML/RARA, FLT3, NPM1, CEBPA)
- AML/ETO Qualitative
- APC gene (Familial Polyposis)
- Array CGH
- Arthrogryposis and Congenital Myasthenic syndrome Gene Panel
- Ataxia Gene Panel
- Autism Gene panel
B
- BCR/ABL (Minor breakpoint) QUALITATIVE
- BCR/ABL by PCR (Major breakpoint)
- BCR/ABL Variant Panel (Mbcr-b2a2, b3a2, b2a3, b3a3; mbcr- e1a2, e1a3; µbcr)
- BCR/ABL1 Kinase Domain Mutation Analysis
- Benign Infantile Epilepsy Gene Panel
- BK/JC Virus PCR Qualitative
- BRAF (V600E)
- BRCA1/2
- Breast and Ovarian Cancer Panel
- Breast Cancer panel
C
- C-KIT Mutation
- C-Myc oncogene (FISH)
- CAH (Congenital Adrenal Hyperplasia) (11 mutations)
- CALR Mutation
- Cancer Panel
- Carbohydrates/Lactose Intolerance
- Cardiac Channelopathy Gene Panel
- Cardiomyopathy Gene Panel
- CEBPA (Full Gene Mutation Analysis)
- Chlamydia PCR Qualitative
- Chromosome 21 (FISH)
- Chromosomes 13, 18, 21,X & Y (FISH)
- Chronic Neutrophilic Leukemia (CSF3R gene)
- Chronic Neutrophilic Leukemia (CSF3R gene; SETBP gene)
- CLL FISH Panel (13q, 17p, 11q, 14q, +12)
- CMV PCR Qualitative
- CMV PCR Quantitative
- Colon Cancer (Fragment Analysis + NGS)
- Common Neurological/neuromuscular diseases
- Complete Inherited Disease Panel
- Congenital Myopathy Gene Panel
- Coronary heart disease (Molecular)
- CYP2C19-Clopidogrel resistance (*2,*3,*4,*10)
- CYP2D6 (Cytochrome P450 2D6) Alleles
- Cystic Fibrosis
D
E
F
- Factor V Leyden
- Familial Mediterranean fever (FMF)
- Fanconi (Chr. Breakage)
- FGFRa
- FISH +12
- FISH +8
- FISH 13q-
- FISH 14q rearrangement
- FISH 4q12 (PDGFA)
- FISH 5q- (5q31;5q33)
- FISH 5q33 (PDGFB)
- FISH 7q-
- FISH ATM (11q22)
- FISH P53 (17p-)
- FISH t(11;14) BCL1/IGH
- FISH t(12;21) TEL/AML
- FISH t(14;16)
- FISH t(14;18) IGH/BCL2
- FISH t(15;17) PML/RARA
- FISH t(16;16) inv16
- FISH t(4;14)
- FISH t(8;21) AML/ETO
- FISH t(9;22) BCR/ABL
- FISH X/Y
- FLT3 (ITD, D835Y)
- FLT3 (Quantitative)
- FMF (MEFV full gene Analysis)
- Fragile X Syndrome (Molecular)
G
H
- Haemophilia A & B gene Panel
- HbE Screening
- HBV PCR Quantitative
- HBV Genotyping
- HBV PCR Qualitative
- HCV Genotyping
- HCV PCR Qualitative
- HCV PCR Quantitative
- Hemochromatosis Common Mutation in HFE Gene
- Hemochromatosis HFE Full Gene Sequencing
- Hemophilia A Common Mutation (Factor VIII Intron 22 and Intron 1 Inversion analysis)
- Her-2 Neu (Ca Breast)
- Hereditary Spastic Paraplegia Gene Panel
- HIV Drug Resistance Genotyping
- HIV PCR Qualitative
- HIV PCR Quantitative
- HIV Proviral DNA
- HLA A, B, C, DR, DQ
- HLA B27 (Molecular)
- HLA typing single
- HLA-B51 (Behcet)
- HLA-B5701 (for abacavir hypersensitivity)
- HPV Genotyping
- HPV PCR Qualitative
- HSV 1 & 2 PCR Qualitative
- Huntington Disease
K
L
M
- Maturity-Onset Diabetes of the Young (MODY) Gene Panel
- MDS Cyto panel (karyo+2 FISH)
- MDS FISH Panel (5q, 7q, +8, 20q)
- Melanoma/Skin Tumors Panel
- MET Amplification (NSCLC) – FISH
- Metabolic Disorder Gene Panel
- MGMT Methylation Assay
- Microcephaly Gene Panel
- Microdeletion Syndrome
- Microdeletion Syndrome Panel + Subtelomeric Deletion/Duplication Panel
- Microsatellite Instability (Colorectal Cancer)
- MLC1 Gene Mutation Analysis (Agrawal Mutation)
- MLL Qualitative
- MPL Mutation
- MPN Panel (Myeloid NGS Panel + BCR/ABL FISH + Karyotyping)
- MPZ Full Length Gene Sequencing (Charcot-Maria- Tooth Disease)
- MTHFR Mutation
- Multicolour FISH
- Multiple Sclerosis (HLA-DRB1*1501)
- Muscular Dystrophy Gene Panel
- Myeloid NGS Panel
- Myotonia Gene Panel
N
P
- P53 Mutation
- Parvovirus B19 PCR Qualitative
- PCM FISH Panel (del(13q), del(17p), t(4;14), t(14;16), 1p/1q)
- PDGFR (Exons 12, 14, 18) (Gastrointestinal Stromal Tumors)
- PDGFR, cKIT(Gastrointestinal Stromal Tumors)
- Perforin NGS Panel
- PGD (Single Embryo)
- PGD (Single Embryo) with maternal DNA contamination check
- PGD (Single gene Disorder)-Baseline
- PGD HLA Typing
- PGS (1-4) Embryo
- PGS (5-6) Embryo
- PGS (7-12) Embryo
- PIK3CA Mutation
- PML/RARA by PCR
- Polycystic Kidney Disease Gene Panel
- Prader-Willi Syndrome (FISH)
- Products of Conception (POC)
- Prostate Cancer Panel
- Prothrombin G20210A Mutation