"CENTER OF MEDICAL GENETICS AND PRIMARY HEALTH CARE" Limited Liability Company (LLC)
Dear user,
Please when connecting with the company, mention "Spyur" as a source of information.
Please also inform us about any inaccuracies in the information by contacting "Spyur".
"CENTER OF MEDICAL GENETICS AND PRIMARY HEALTH CARE" Limited Liability Company (LLC)
View on the map- Executive
-
Tamara F. Sarkisian, Director
- Contact information
- send mail
- Site
- Find us on
- Short address of the current page
- Spyur.am/medgen
Dear user,
Please when connecting with the company, mention "Spyur" as a source of information.
Please also inform us about any inaccuracies in the information by contacting "Spyur".
Activity
Molecular and clinical diagnosis of hereditary diseases
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- Products, services by "Spyur's" classifier
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- 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 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)
- Complete Blood Count (CBC) for White Blood Cells
- 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
- Treatment Methods
- Treatment of Diseases
- Various Health Services
- Medical Advice/Consultations
- Public Health
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- Activity types by "Spyur's" classifier
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- COMPANIES AND NON-PROFIT ORGANIZATIONS
- PUBLIC HEALTH
- COMPANIES AND NON-PROFIT ORGANIZATIONS
Other information
- Number of employees
- From 16 to 50
- Form of ownership
- Non-governmental
- Year established
- 1998
- Date of information update
- 16.09.2022
- GENETIKAI AXTOROSHMAN KENTRON
- CENTER OF MEDICAL GENETICS
- | 5-Fluorouracil Sensitivity Testing
- | 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
- | Complete Blood Count CBC for White Blood Cells, FBC, full blood count | Complete blood test CBC for White Blood Cells | Complete Blood Count FBC for White Blood Cells | Complete Blood Count full blood count for White Blood Cells
- | Cytogenetic Diagnosis diagnostics
- | Prevention of Gynecological Diseases, gynecology | Prevention of gynecology Diseases
- | 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
- | 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, & | Molecular & Cytogenetic Diagnosis of Leukemia
- | Consulting on Gynecological Diseases Gynecologist's Consultation, gynecology | Consulting on gynecology Diseases Gynecologist's Consultation
- | Lactose Intolerance Test
- MEDICAL DIAGNOSTIC CENTERS LABORATORIES
- | Breast Cancer Genetic Testing
- | Antibiotics Sensitivity Testing
- | Comprehensive Diagnosis of Anti-Phospholipid Syndrome diagnostics
- | Postnatal Diagnosis diagnostics
- | Cytogenetic Diagnosis of Recurrent Miscarriage Pregnancy Loss diagnostics
- | Breast Cancer Hormone Therapy Sensitivity Testing
- | Ovarian Cancer Genetic Testing
- | Molecular Diagnosis of Predisposition to Thrombosis diagnostics
- Genotyping of Human Papilloma Virus
- | Molecular Diagnosis diagnostics
- Identification Detection of DNA RNA Infectious Agents Using DNA-Microarrays (DNA Chips Biochips)
- | Intellectual Disability Genetic Testing
- | Molecular Diagnosis of Mucoviscidosis Cystic Fibrosis diagnostics
- | Prenatal Diagnosis diagnostics
- Prenatal Diagnosis in I & II Trimesters of Pregnancy
- | 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
- | Molecular Diagnosis of Infections diagnostics
- | Warfarin Sensitivity Testing
- | Cytogenetic Diagnosis of Chromosomal Syndromes diagnostics
- MEDICAL DIAGNOSTIC LABS MEDICAL DIAGNOSTIC LAB | MEDICAL DIAGNOSTIC CENTER (LABORATORY), centre
- MEDICAL CENTERS
- MEDICAL CENTERS
- MEDICAL CENTERS
- MEDICAL DIAGNOSTIC CENTERS
- MEDICAL DIAGNOSTIC LABORATORIES
- MEDICAL DIAGNOSTIC CENTER
- MEDICAL DIAGNOSTIC CENTERS
- MEDICAL DIAGNOSTIC LABORATORY
- MEDICAL DIAGNOSTIC CENTER
- MEDICAL DIAGNOSTIC LABORATORY
- MEDICAL DIAGNOSTIC LABORATORIES
- CLINICS
- CLINICS
- 225
- T 602/184
- 15.05.2001
- 01.10.22 -
- 6000
