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/

Submissions in ClinVar
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GTR Lab ID: 505783, Last updated:2024-02-05

Personnel

Director: Mohammad Miryounesi, PhD, MD, Lab Director
Phone: +982122439959
Fax: +982122439961
Email: miryounesi@sbmu.ac.ir
Director: Hassan Roudgari, PhD, MD, Lab Director
Email: h.roudgari@sbmu.ac.ir

Conditions and tests

49 conditions/phenotypes with 21 tests
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alpha Thalassemia1 test
Autoimmune lymphoproliferative syndrome type 11 test
Autosomal hypohidrotic ectodermal dysplasia2 tests
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 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
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
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
Trisomy 181 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.