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Genomic Research Center

  • Genomic Research Center, GRC
  • Shahid Beheshti University of Medical Sciences (SBMU)
  • Department: Genomic Research Center / National Center for Genomic Excellence
  • Taleghani General Hospital, Araabi St., Yaman Ave.,, Velenjak, Evin
  • Tehran, Tehran, Iran 1985717413
  • Phone: +982122433580
    Fax: +982122433583
    Email: v.yassaee-grc@sbmu.ac.ir
  • Website: http://grc.sbmu.ac.ir
  • Affiliated with:
    • Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran, http://grc.sbmu.ac.ir/
    • National Center for Genomic Excellence, Shahid Beheshti University of Medical Sciences, Tehran, Iran

GTR Lab ID: 504864, Last updated:2020-03-10

Personnel

Conditions and tests

  • Acute lymphoid leukemia1 test
  • Acute myeloid leukemia1 test
  • Acute myeloid leukemia, M6 type1 test
  • Acute myelomonocytic leukemia M41 test
  • Acute promyelocytic leukemia1 test
  • alpha Thalassemia1 test
  • Autoimmune lymphoproliferative syndrome1 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
  • Burkitt lymphoma1 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
  • Chronic lymphocytic leukemia1 test
  • Chronic myelogenous leukemia, BCR-ABL1 positive1 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
  • Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant1 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 and 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
  • Leukemia, post-chemotherapy, susceptibility to1 test
  • Limb-girdle muscular dystrophy, type 1B1 test
  • Lissencephaly due to LIS1 mutation1 test
  • Lymphoid leukemia1 test
  • Mandibuloacral dysplasia with type A lipodystrophy1 test
  • Miller Dieker syndrome1 test
  • MTHFR deficiency, thermolabile type1 test
  • not provided1 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 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

  • Confirmation of research findings
  • Custom Sequence Analysis
  • Carrier testing
  • DNA Banking
  • Mutation Confirmation
  • RNA Banking

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