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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, http://ccgs.sbmu.ac.ir/

GTR Lab ID: 505783, Last updated:2022-04-17

Personnel

Conditions and tests

  • alpha Thalassemia1 test
  • Autoimmune lymphoproliferative syndrome type 11 test
  • Autosomal hypohidrotic ectodermal dysplasia2 tests
  • Benign scapuloperoneal muscular dystrophy with cardiomyopathy1 test
  • Beta thalassemia intermedia1 test
  • Beta-thalassemia major1 test
  • Breast cancer, early-onset1 test
  • Breast cancer, familial male1 test
  • Breast-ovarian cancer, familial, susceptibility to, 11 test
  • Charcot-Marie-Tooth disease type 2B11 test
  • Chromosome 16 trisomy1 test
  • Chromosome 22q11.2 deletion syndrome, distal1 test
  • Chromosome 22q11.2 microduplication syndrome1 test
  • Complete trisomy 13 syndrome1 test
  • Complete trisomy 18 syndrome1 test
  • Complete trisomy 21 syndrome1 test
  • Congenital muscular dystrophy due to LMNA mutation1 test
  • Cystic fibrosis1 test
  • Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1 test
  • Dilated cardiomyopathy 1A1 test
  • Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant1 test
  • Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive1 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 H disease1 test
  • Hereditary breast ovarian cancer syndrome1 test
  • Hereditary thrombophilia1 test
  • Huntington disease1 test
  • Hutchinson-Gilford progeria syndrome, childhood-onset1 test
  • HYDROPS FETALIS, ALPHA-THALASSEMIA-RELATED1 test
  • Lethal tight skin contracture syndrome1 test
  • Lissencephaly due to LIS1 mutation1 test
  • Mandibuloacral dysplasia with type A lipodystrophy1 test
  • Miller Dieker syndrome1 test
  • MTHFR THERMOLABILE POLYMORPHISM1 test
  • Prader-Willi syndrome1 test
  • Smith-Magenis syndrome1 test
  • Steinert myotonic dystrophy syndrome1 test
  • Succinate-semialdehyde dehydrogenase deficiency1 test
  • Thalassemia intermedia1 test
  • Thalassemia minor1 test
  • Thrombophilia due to activated protein C resistance1 test
  • Thrombophilia due to thrombin defect1 test
  • Thrombophilia, familial, due to decreased release of tissue plasminogen activator1 test
  • Turner syndrome1 test
  • Williams syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Balanced Chromosome Rearrangement Studies
  • Custom Deletion/Duplication Testing
  • Prenatal testing
  • Custom Sequence Analysis
  • Carrier testing
  • DNA Banking
  • Genetic counseling
  • Marker Chromosome Identification
  • Mutation Confirmation
  • Whole Exome Sequencing

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.