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"CENTER OF MEDICAL GENETICS AND PRIMARY HEALTH CARE" Limited Liability Company (LLC)
ISO certified center
Contact information
Executive
Tamara F. Sarkisian, Director
Address, telephones
Armenia, 0009, Yerevan
Abovyan St., 34/3 Building (opposite "Poqr Pariz" cafe)
(Kentron adm. district)
Mon Tue Wed Thu Fri 08:30-18:00
Sat 09:30-13:30
•
+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
Find us on
Spyur
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.
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"Spyur"
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Activity
Molecular and clinical diagnosis of hereditary diseases
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
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 Blood Test for White Blood Cells
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/Analysis (Urinalysis/UA)
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
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
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
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 Examination
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 Analysis
Smear Test
Smear Test for Demodex
Study of Hemostasis System (Coagulation Tests/Blood Clotting Tests)
Testing for Rheumatoid Factor
Warfarin Sensitivity Testing
Prevention of Diseases
Prevention of Gynecological Diseases
Prevention of Uterine Cervical Neoplasms/Tumors
Treatment Methods
Benign Skin Neoplasm/Tumor Removal
Chemical Destruction
Cryodestruction/Cryoablation
Electrocoagulation
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 of Development of Hereditary Diseases
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
07.09.2020
Some keywords
GENETIKAI AXTOROSHMAN KENTRON
centre CENTER OF MEDICAL GENETICS AND PRIMARY HEALTH CARE
CENTER OF MEDICAL GENETICS
| 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
| Treatment of Allergic Diseases Allergist Services therapy service
| Cytogenetic Diagnosis diagnostics
| Prevention of Gynecological Diseases gynaecological
| Prenatal Diagnosis of Down Syndrome Using FISH fluorescent in situ hybridization Method diagnostics
| Clinical Diagnosis of Duchenne-Becker Muscular Dystrophy Myodystrophy diagnostics
| Molecular Diagnosis of Duchenne-Becker Muscular Dystrophy Myodystrophy diagnostics
| Prenatal Diagnosis of Edwards Syndrome Using FISH fluorescent in situ hybridization Method diagnostics
| DNA Diagnosis of Hereditary Diseases diagnostics
| Molecular Genetic Diagnosis of Hereditary Diseases diagnostics
| Clinical Diagnosis of Gilbert's Syndrome Hereditary Bilirubinemia diagnostics
| Molecular Diagnosis of Gilbert's Syndrome Hereditary Bilirubinemia diagnostics
| Invasive Prenatal Diagnosis diagnostics
| Molecular and Cytogenetic Diagnosis of Leukemia 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
MEDICAL DIAGNOSTIC CENTERS LABORATORIES | Clinical Laboratory Services service
| Comprehensive Diagnosis of Anti-Phospholipid Syndrome diagnostics
| Postnatal Diagnosis diagnostics
| Cytogenetic Diagnosis of Recurrent Miscarriage Pregnancy Loss diagnostics
| Molecular Diagnosis of Predisposition to Thrombosis diagnostics
Genotyping of Human Papilloma Virus
| Molecular Diagnosis of Monogenic Hereditary Diseases diagnostics
| Molecular Diagnosis diagnostics
Identification/Detection of DNA/RNA Infectious Agents Using DNA-Microarrays (DNA Chips/Biochips)
| Molecular Diagnosis of Mucoviscidosis Cystic Fibrosis diagnostics
| Prenatal Diagnosis diagnostics
| Prenatal Diagnosis in I and II Trimesters of Pregnancy diagnostics
| Ultrasound Examination Sonography Echography Internal Organs ultrasonic
| Comprehensive Laboratory Diagnosis of Diabetes diagnostics
| Clinical Diagnosis of Spinal Amyotrophy diagnostics
| Molecular Diagnosis of Spinal Amyotrophy diagnostics
| Non-Invasive Prenatal Diagnosis diagnostics
| Cytogenetic Diagnosis of Infertility diagnostics
| Prenatal Diagnosis of Patau Syndrome Using FISH fluorescent in situ hybridization Method diagnostics
| Prenatal Diagnosis of Fetal Congenital Malformations diagnostics
| Molecular Diagnosis of Infections diagnostics
| Clinical Diagnosis of Male Infertility diagnostics
| Molecular Diagnosis of Male Infertility diagnostics
| Cytogenetic Diagnosis of Chromosomal Syndromes diagnostics
| 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
T 554/225, W 19534
15.05.2001
01.10.20 -
6000
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