BUSINESS MESSAGE

5-Fluorouracil Sensitivity Testing

Analysis of Gene Mutations in Hereditary Breast/Ovarian Cancer

Antibiotics Sensitivity Testing

Biochemical Blood Analysis

Biochemical Blood Test

Blood Coagulation Testing

Breast Cancer Genetic Testing

Breast Cancer Hormone Therapy Sensitivity Testing

Cervical Smear Cytological Examination (Pap Test)

Clinical Diagnosis of Duchenne-Becker Muscular Dystrophy (Myodystrophy)

Clinical Diagnosis of Gilbert's Syndrome (Hereditary Bilirubinemia)

Clinical Diagnosis of Male Infertility

Clinical Diagnosis of Spinal Amyotrophy

Clinical Genetic Diagnosis of Periodic Peritonitis

Clinical Laboratory Services

Clinical Urine Test (Urinalysis/UA)

Complete Blood Count (CBC) with Differential

Comprehensive Diagnosis of Anti-Phospholipid Syndrome

Comprehensive Examination of Pregnant Women

Comprehensive Examination of Sexual and Reproductive System

Comprehensive Laboratory Diagnosis of Diabetes

Cytogenetic Diagnosis

Cytogenetic Diagnosis of Chromosomal Syndromes

Cytogenetic Diagnosis of Infertility

Cytogenetic Diagnosis of Recurrent Miscarriage/Pregnancy Loss

Detection of Human Enteric Virus (Enterovirus)

Detection of Human Herpes Virus (Herpesvirus)

Detection of Tumor Markers

DNA Diagnosis of Hereditary Diseases

Early Non-Invasive Prenatal Screening

Genetic Testing

Genotyping of Human Papillomavirus

Hemostasis Testing (Coagulation Tests)

Hormonal Laboratory Examinations

Immunohistochemical Examinations

Immunohistochemical Testing of Hormone Receptors in Oncological Diseases (Neoplasms/Tumors)

Immunological Diagnosis of Infections

Immunological Laboratory Examinations

Intellectual Disability Genetic Testing

Internal Organs Ultrasound Examination (Sonography/Echography)

Invasive Prenatal Diagnosis

Lactose Intolerance Test

Molecular and Cytogenetic Diagnosis of Leukemia

Molecular Diagnosis

Molecular Diagnosis of Allergy by ImmunoCAP Method

Molecular Diagnosis of Duchenne-Becker Muscular Dystrophy (Myodystrophy)

Molecular Diagnosis of Gilbert's Syndrome (Hereditary Bilirubinemia)

Molecular Diagnosis of Infections

Molecular Diagnosis of Male Infertility

Molecular Diagnosis of Monogenic Hereditary Diseases

Molecular Diagnosis of Mucoviscidosis (Cystic Fibrosis)

Molecular Diagnosis of Predisposition to Thrombosis

Molecular Diagnosis of Spinal Amyotrophy

Molecular Genetic Diagnosis of Hereditary Diseases

Molecular Genetic Testing for Identification of DNA/RNA Infectious Agents by Polymerase Chain Reaction (PCR) Method Using DNA-Microarrays (DNA Chips/Biochips)

Monitoring: Pharmacotherapy

Non-Invasive Prenatal Diagnosis

Oncogenetic Testing

Ovarian Cancer Genetic Testing

Postnatal Diagnosis

Prenatal Diagnosis

Prenatal Diagnosis in I and II Trimesters of Pregnancy

Prenatal Diagnosis of Aneuploidy of X-Chromosomes Using FISH (fluorescent in situ hybridization) Method

Prenatal Diagnosis of Aneuploidy of Y-Chromosomes Using FISH (fluorescent in situ hybridization) Method

Prenatal Diagnosis of Down Syndrome Using FISH (fluorescent in situ hybridization) Method

Prenatal Diagnosis of Edwards Syndrome Using FISH (fluorescent in situ hybridization) Method

Prenatal Diagnosis of Fetal Congenital Malformations

Prenatal Diagnosis of Patau Syndrome Using FISH (fluorescent in situ hybridization) Method

Semen/Ejaculate Analysis

Smear Test

Smear Test for Demodex

Testing for Rheumatoid Factor

Warfarin Sensitivity Testing

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"CENTER OF MEDICAL GENETICS AND PRIMARY HEALTH CARE"

Tamara Sarkisian, Director

Dear Tamara Sarkisian

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