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Laboratory Services


Molecular Genetic Laboratory

The department of molecular genetics provides prenatal and postnatal genetic diagnosis of common and rare hereditary disorders, genetic testing of multifactorial diseases, pharmacogenetic testing of genetic polymorphisms relevant for the treatment of different types of diseases, patient and presymptomatic testing of hereditary forms of cancer, and detection of infections by using different techniques of molecular genetics.


Tests
Familial Mediterranean Fever (FMF) - MEFV 30 000 AMD
Duchenne and Becker Muscular Dystrophies (DMD and BMD) – DMD 20 000 AMD
Cardiovascular (CVD), Thrombophilia risk factors (8 mutations/polymorphisms) 30 000 AMD
Congenital Adrenal Hyperplasia (CAH) - CYP21A2 30 000 AMD
Cystic Fibrosis (CF) - CFTR 30 000 AMD
Cystic Fibrosis (CF) - CFTR (prenatal) 55 000 AMD
Spinal Muscular Atrophy (SMA) - SMN1 20 000 AMD
Spinal Muscular Atrophy (SMA) - SMN1 (prenatal) 45 000 AMD
Fragile X Syndrome (FRAX) - FMR1 20 000 AMD
Lyme disease (Lyme borreliosis, LB) 12 000 AMD
Alpha Thalassemia (α-Thal) – α1, α2 45 000 AMD
Alpha Thalassemia (α-Thal) – α1, α2 (prenatal) 70 000 AMD
Beta Thalassemia (β-Thal) - β1 40 000 AMD
Beta Thalassemia (β-Thal) - β1 (prenatal) 65 000 AMD
Irinotecan dosing – UGT1A1 15 000 AMD
Gilbert Syndrome (GS) – UGT1A1 15 000 AMD
5-fluorouracil treatment relevance (5-FU) - DPYD1 20 000 AMD
Hereditary Syndrome of Brest and Ovarian Cancer: BRCA 1&2 genes examination 265 000 AMD
Detection of BRCA gene mutations in ovarian cancer cells. Detection of targeted treatment sensitivity (Lynparza – olaparib) 285 000 AMD
Warfarin (Coumarin) anticoagulant therapy optimization -VKORC1 and CYP2C9 30 000 AMD
Ureaplasma parvum & urealiticum 6 000 AMD
Micoplasma genitalium 6 000 AMD
Micoplasma hominis 6 000 AMD
Chlamidia trachomatis 6 000 AMD
Neisseria gonorrhoeae 6 000 AMD
Trichomonas vaginalis 6 000 AMD
Gardnerella vaginalis 6 000 AMD
Human Cytomegalovirus 6 000 AMD
Human Herpes Simplex Virus 1&2 6 000 AMD
Epstein-Barr Virus 6 000 AMD
Assessment of Renal Amyloidosis development risk among patients with Familial Mediterranean Fever (FMF) – SAA1 gene 20 000 AMD
HLA-B27 antigene PCR 30 000 AMD
Haemochromatosis 30 000 AMD
Azoospermia and Oligospermia - Y chromosome microdeletions test 15 000 AMD
Human PapilomaVirus 6&11 6 000 AMD
Human PapilomaVirus 16&18 6 000 AMD
Human PapilomaVirus 31&33 6 000 AMD
Human PapilomaVirus 35&45 6 000 AMD
Consanguinity (paternity, maternity) detection 200 000 AMD
Non-Invasive Prenatal Testing (NIPT) 260 000 AMD
Congenital absence of Vas Deferens - CFTR test 30 000 AMD
Mutations of FII and FV factors of Coagulation and MTHFR 30 000 AMD
Staff

Davit Babikyan


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