ISO certified center

Contact information

• Executive
• Tamara F. Sarkisian, Director
• Address, telephone
• Armenia, 0009, Yerevan
  Abovyan St., 34/3 Building (opposite "Poqr Pariz" cafe)

  (Kentron adm. district)

  Mon Tue Wed Thu Fri Sat(half day) 09:00-17:00

  • +374-10-544367 , +374-10-544366 , +374-99-544366 (mobile)
• Other communications
• • Fax: +374-10-544366
• E-mail
• • send mail
  Price request

  Free message
• Site
• http://www.cmg.am
• Short address of the current page
• Spyur.am/medgen




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Please when connecting with the company, mention "Spyur" as a source of information. Please also inform us about any inaccuracies in the information by calling at 113 phone number.

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Activity

• Molecular and clinical diagnosis of hereditary diseases
  

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• Products, services by "Spyur" classifier
• • Public Health
    • Medical Advice/Consultations
      • Consulting on Andrologic Diseases / Andrologist's Consultation
      • Consulting on Cardiovascular Diseases / Cardiologist's Consultation
      • Consulting on Genetic Diseases of Nervous System
      • Consulting on Gynecological Diseases / Gynecologist's Consultation
      • Consulting on Internal Diseases / Therapist's Consultation
      • Consulting on Rheumatic Diseases / Rheumatologist's Consultation
      • Consulting on Urologic Diseases / Urologist's Consultation
      • Genetic Consultations
    • Medical Examination
      • Analysis of Gene Mutations in Hereditary Breast/Ovarian Cancer
      • Biochemical Blood Analysis
      • Blood Coagulation Testing
      • Blood Test: Biochemical
      • Blood Test for White Blood Cells: Clinical
      • 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
      • Comprehensive Diagnosis of Anti-Phospholipid Syndrome
      • Comprehensive Examination of Pregnant Women
      • Comprehensive Examination of 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
      • Cytological Examination: Cervical Smear (Pap Test)
      • 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 Examination
      • Genetic Testing: Breast Cancer
      • Genetic Testing: Intellectual Disability
      • Genetic Testing: Ovarian Cancer
      • Genotyping of Human Papillomavirus
      • Hormonal Laboratory Examination
      • Immunohistochemical Examination
      • Immunohistochemical Testing of Hormone Receptors in Oncological Diseases (Neoplasms/Tumors)
      • Immunological Diagnosis of Infections
      • Immunological Laboratory Examination
      • 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 Examination
      • 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 Analysis
      • Sensitivity Testing: 5-Fluorouracil
      • Sensitivity Testing: Antibiotics
      • Sensitivity Testing: Hormonotherapy of Breast Cancer
      • Sensitivity Testing: Warfarin
      • Smear Test
      • Smear Test for Demodex
      • Study of Hemostasis System (Coagulation Tests/Blood Clotting Tests)
      • Testing for Rheumatoid Factor
      • Ultrasound Examination (Sonography/Echography): Internal Organs
      • Urine Test/Analysis: Clinical (Urinalysis/UA)
    • Prevention of Diseases
      • Prevention of Gynecological Diseases
      • Prevention of Uterine Cervical Neoplasms/Tumors
    • Treatment Methods
      • Chemical Destruction
      • Cryodestruction/Cryoablation
      • Electrocoagulation
      • Removal of Benign Skin Neoplasms (Tumors)
    • Treatment of Diseases
      • Treatment of Allergic Diseases / Allergist Services
      • Treatment of Periodic Peritonitis
      • Treatment of Various Internal Diseases / Therapist Services
    • Various Health Services
      • Biomaterial Sampling for Laboratory Analysis: on Call (in-home)
      • DNA Bank Services
      • Forecasting: Development of Hereditary Diseases

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• Types of activity by "Spyur" classifier
• • COMPANIES AND NON-PROFIT ORGANIZATIONS
    • PUBLIC HEALTH
      • HOSPITAL / CLINIC / MEDICAL CENTER
      • MEDICAL DIAGNOSTIC CENTER (LABORATORY)

Other information

• Number of employees
• From 16 to 50
• Form of ownership
• Non-governmental
• Year established
• 1998
• Date of information update
• 31.01.2019
• Some keywords 
• GENETIKAI AXTOROSHMAN KENTRON
• centre
• CENTER OF MEDICAL GENETICS
• | Cytogenetic Diagnosis diagnostics
• | Cytogenetic Diagnosis of Recurrent Miscarriage Pregnancy Loss diagnostics
• | Cytogenetic Diagnosis of Infertility diagnostics
• | Cytogenetic Diagnosis of Chromosomal Syndromes diagnostics
• | Treatment of Allergic Diseases Allergist Services therapy service
• Genotyping of Human Papilloma Virus
• | DNA Diagnosis of Hereditary Diseases diagnostics
• | Invasive Prenatal Diagnosis diagnostics
• | Consulting on Andrologic Diseases Andrologist's Consultation advice
• | Consulting on Gynecological Diseases Gynecologist's Consultation advice gynaecological
• | Consulting on Internal Diseases Therapist's Consultation advice
• | Consulting on Genetic Diseases of Nervous System advice
• | Consulting on Cardiovascular Diseases Cardiologist's Consultation advice
• | Consulting on Urologic Diseases Urologist's Consultation advice
• | Prevention of Gynecological Diseases gynaecological
• | Clinical Diagnosis of Duchenne-Becker Muscular Dystrophy Myodystrophy diagnostics
• | Clinical Diagnosis of Gilbert's Syndrome Hereditary Bilirubinemia diagnostics
• | Clinical Diagnosis of Spinal Amyotrophy diagnostics
• | Clinical Diagnosis of Male Infertility diagnostics
• MEDICAL DIAGNOSTIC CENTERS LABORATORIES | Clinical Laboratory Services service
• | Comprehensive Diagnosis of Anti-Phospholipid Syndrome diagnostics
• | Comprehensive Laboratory Diagnosis of Diabetes diagnostics
• | Postnatal Diagnosis diagnostics
• | Molecular Diagnosis diagnostics
• | Molecular Diagnosis of Duchenne-Becker Muscular Dystrophy Myodystrophy diagnostics
• | Molecular Diagnosis of Gilbert's Syndrome Hereditary Bilirubinemia diagnostics
• | Molecular Diagnosis of Predisposition to Thrombosis diagnostics
• | Molecular Diagnosis of Monogenic Hereditary Diseases diagnostics
• | Molecular Diagnosis of Mucoviscidosis Cystic Fibrosis diagnostics
• | Molecular Diagnosis of Spinal Amyotrophy diagnostics
• | Molecular Diagnosis of Infections diagnostics
• | Molecular Diagnosis of Male Infertility diagnostics
• | Molecular and Cytogenetic Diagnosis of Leukemia diagnostics
• | Molecular Genetic Diagnosis of Hereditary Diseases diagnostics
• Identification/Detection of DNA/RNA Infectious Agents Using DNA-Microarrays (DNA Chips/Biochips)
• | Prenatal Diagnosis diagnostics
• | Prenatal Diagnosis of Aneuploidy of X-Chromosomes Using FISH fluorescent in situ hybridization Method diagnostics
• | Prenatal Diagnosis of Aneuploidy of Y-Chromosomes Using FISH fluorescent in situ hybridization Method diagnostics
• | Prenatal Diagnosis of Down Syndrome Using FISH fluorescent in situ hybridization Method diagnostics
• | Prenatal Diagnosis of Edwards Syndrome Using FISH fluorescent in situ hybridization Method diagnostics
• | Prenatal Diagnosis in I and II Trimesters of Pregnancy diagnostics
• | Prenatal Diagnosis of Patau Syndrome Using FISH fluorescent in situ hybridization Method diagnostics
• | Prenatal Diagnosis of Fetal Congenital Malformations diagnostics
• | Non-Invasive Prenatal Diagnosis diagnostics
• | Ultrasound Examination Sonography Echography Internal Organs ultrasonic
• | HOSPITALS CLINICS MEDICAL CENTERS clinic
• MEDICAL DIAGNOSTIC LABS MEDICAL DIAGNOSTIC LAB
• MEDICAL CENTERS
• CLINICS
• HOSPITALS
• CLINIC
• MEDICAL CENTER
• MEDICAL CENTERS
• MEDICAL CENTER
• MEDICAL DIAGNOSTIC CENTER
• MEDICAL DIAGNOSTIC LABORATORY
• MEDICAL DIAGNOSTIC CENTERS
• MEDICAL DIAGNOSTIC LABORATORIES
• 225
• T0
• 5375