GTR Home > Laboratories > Center for Comprehensive Genetic Services

Center for Comprehensive Genetic Services

  • Center for Comprehensive Genetic Services, CCGS
  • Shahid Beheshti University of Medical Sciences (SBMU)
  • Taleghani General Hospital, Araabi St., Yaman Ave., Velenjak, Evin
  • Tehran, Tehran, Iran 1985717413
  • Phone: +982122439959
    Fax: +982122439961
    Email: ccgs@sbmu.ac.ir
  • Website: http://ccgs.sbmu.ac.ir/
  • Affiliated with:
    • Center for Comprehensive Genetic Services, Shahid Beheshti University of Medical Sciences, Tehran, Iran

GTR Lab ID: 505783, Last updated:2018-04-21

Personnel

Conditions and tests

  • 22q11.2 duplication syndrome1 test
  • alpha Thalassemia1 test
  • Autoimmune lymphoproliferative syndrome1 test
  • Autosomal dominant hypohidrotic ectodermal dysplasia1 test
  • Autosomal hypohidrotic ectodermal dysplasia2 tests
  • Autosomal recessive hypohidrotic ectodermal dysplasia syndrome1 test
  • Beta thalassemia intermedia1 test
  • Beta thalassemia major1 test
  • Beta thalassemia minor1 test
  • Breast cancer, early-onset1 test
  • Breast cancer, familial male1 test
  • Breast-ovarian cancer, familial 11 test
  • Charcot-Marie-Tooth disease type 2B11 test
  • Chromosome 16, trisomy1 test
  • Chromosome 22q11.2 deletion syndrome, distal1 test
  • Complete trisomy 13 syndrome1 test
  • Complete trisomy 18 syndrome1 test
  • Complete trisomy 21 syndrome1 test
  • Congenital muscular dystrophy, LMNA-related1 test
  • Cystic fibrosis1 test
  • Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1 test
  • Dilated cardiomyopathy 1A1 test
  • Emery-Dreifuss muscular dystrophy 3, autosomal recessive1 test
  • Fanconi anemia1 test
  • Glucocorticoid deficiency with achalasia1 test
  • Hb SS disease1 test
  • Heart-hand syndrome, Slovenian type1 test
  • Hemoglobin H1 test
  • Hereditary breast and ovarian cancer syndrome1 test
  • Hereditary thrombophilia1 test
  • Huntington's chorea1 test
  • Hutchinson-Gilford progeria syndrome, childhood-onset1 test
  • HYDROPS FETALIS, ALPHA-THALASSEMIA-RELATED1 test
  • Lethal tight skin contracture syndrome1 test
  • Limb-girdle muscular dystrophy, type 1B1 test
  • Lissencephaly 11 test
  • Mandibuloacral dysostosis1 test
  • Miller Dieker syndrome1 test
  • MTHFR deficiency, thermolabile type1 test
  • Prader-Willi syndrome1 test
  • Smith-Magenis syndrome1 test
  • Steinert myotonic dystrophy syndrome1 test
  • Succinate-semialdehyde dehydrogenase deficiency1 test
  • Thalassemia intermedia1 test
  • Thrombophilia due to factor V Leiden1 test
  • Thrombophilia, familial, due to decreased release of tissue plasminogen activator1 test
  • Turner syndrome1 test
  • Venous thrombosis1 test
  • Williams syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Balanced Chromosome Rearrangement Studies
  • Prenatal testing
  • Custom Sequence Analysis
  • Carrier testing
  • Genetic counseling
  • Marker Chromosome Identification
  • Mutation Confirmation

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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