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

Submissions in ClinVar
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GTR Lab ID: 504864, Last updated:2024-02-27

Personnel

Director: Vahid Yassaee, PhD, MD, Lab Director
Phone: +982122433580
Fax: +982122433583
Email: v.yassaee-grc@sbmu.ac.ir
Farzad Hashemi-Gorji, MS, MSc, Lab Associate Director
Phone: 0098-212-243-9959
Fax: 0098-212-243-9961
Email: f.hashemi-grc@sbmu.ac.ir

Conditions and tests

60 conditions/phenotypes with 22 tests
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Acute lymphoid leukemia1 test
Acute myeloid leukemia1 test
Acute myelomonocytic leukemia M41 test
Acute promyelocytic leukemia1 test
alpha Thalassemia1 test
Autoimmune lymphoproliferative syndrome type 11 test
Autosomal hypohidrotic ectodermal dysplasia2 tests
B-cell chronic lymphocytic leukemia1 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
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 myelogenous leukemia, BCR-ABL1 positive1 test
Classic Hodgkin lymphoma1 test
Complete trisomy 13 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 2, autosomal dominant1 test
Emery-Dreifuss muscular dystrophy 3, autosomal recessive1 test
Erythroleukemia, familial, susceptibility to1 test
Fanconi anemia1 test
Glucocorticoid deficiency with achalasia1 test
Hb SS disease1 test
Heart-hand syndrome, Slovenian type1 test
Hemoglobin Bart hydrops syndrome1 test
Hemoglobin H disease1 test
Hereditary breast ovarian cancer syndrome1 test
Hereditary thrombophilia1 test
Huntington disease1 test
Hutchinson-Gilford progeria syndrome, childhood-onset1 test
Lethal tight skin contracture syndrome1 test
Leukemia, post-chemotherapy, susceptibility to1 test
Lissencephaly due to LIS1 mutation1 test
Lymphoid leukemia1 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
Trisomy 181 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

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.