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GTR Home > Laboratories > Center for Genetics at Saint Francis

Center for Genetics at Saint Francis

GTR Lab ID: 1063, Last updated:2021-11-23
Annual Review past due read more


  • Director: Khadija Belhassan, MD, Lab Director
    Phone: 918-502-1726
    Fax: 918-502-1723
    Email: kbelhassan@saintfrancis.com
  • Director: Kavita Reddy, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
    Phone: United States
    Fax: 918-502-1723
    Email: ksreddy@saintfrancis.com
  • Lynne Whetsell, BS, MB(ASCP), Administrator
    Phone: 918-502-1730
    Fax: 918-502-1723
    Email: lhwhetsell@saintfrancis.com

Conditions and tests

  • Achondroplasia1 test
  • Acrocephalosyndactyly type I3 tests
  • Albright hereditary osteodystrophy1 test
  • Aminoglycoside-induced deafness2 tests
  • Amyotrophic lateral sclerosis type 11 test
  • Androgen resistance syndrome1 test
  • Angelman syndrome1 test
  • Antley-Bixler syndrome2 tests
  • Autosomal dominant nonsyndromic hearing loss 3A3 tests
  • Autosomal recessive nonsyndromic hearing loss 1A3 tests
  • Blau syndrome1 test
  • Crouzon syndrome2 tests
  • Crouzon syndrome-acanthosis nigricans syndrome1 test
  • Cystic fibrosis1 test
  • Dentatorubral-pallidoluysian atrophy1 test
  • Familial scaphocephaly syndrome, McGillivray type2 tests
  • Fragile X syndrome1 test
  • Friedreich ataxia 11 test
  • Frontotemporal dementia3 tests
  • GRN-related frontotemporal lobar degeneration with Tdp43 inclusions1 test
  • Hereditary ataxia1 test
  • Huntington disease1 test
  • Hypochondroplasia1 test
  • Inflammatory bowel disease 11 test
  • Jackson-Weiss syndrome2 tests
  • Kugelberg-Welander disease1 test
  • Li-Fraumeni syndrome 11 test
  • Loeys-Dietz syndrome 12 tests
  • Marfan syndrome3 tests
  • MASS syndrome3 tests
  • McCune-Albright syndrome1 test
  • Muenke syndrome3 tests
  • Neural tube defects, folate-sensitive1 test
  • Pendred syndrome1 test
  • Pfeiffer syndrome2 tests
  • Prader-Willi syndrome2 tests
  • Progressive osseous heteroplasia1 test
  • Pseudohypoparathyroidism1 test
  • Pseudopseudohypoparathyroidism1 test
  • Saethre-Chotzen syndrome2 tests
  • Severe short stature1 test
  • Shprintzen-Goldberg syndrome2 tests
  • Spinal muscular atrophy, type II1 test
  • Spinocerebellar ataxia 71 test
  • Spinocerebellar ataxia type 11 test
  • Spinocerebellar ataxia type 21 test
  • Spinocerebellar ataxia type 61 test
  • Steinert myotonic dystrophy syndrome1 test
  • Stiff skin syndrome3 tests
  • Thrombophilia due to activated protein C resistance1 test
  • Thrombophilia due to thrombin defect1 test
  • Waardenburg syndrome type 11 test
  • Waardenburg syndrome type 2A1 test
  • Waardenburg syndrome type 31 test
  • Werdnig-Hoffmann disease1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously

List of certifications/licenses


  • CLIAHelp, Number: 37D0474681, Expiration date: 2022-10-19
  • CAP, Number: 2050201, Expiration date: 2021-12-10


  • CA - California Department of Public Health CDPH, Number: COS 00800312, Expiration date: 2022-08-16
  • PA - Pennsylvania Department of Health PADOH, Number: 033970, Expiration date: 2022-08-15

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.