Center for Genetics at Saint Francis

Personnel

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

55 conditions/phenotypes with 42 tests
Enter text to narrow down the list

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
Craniofacial dysostosis2 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

Certifications

CLIAHelpCertification number assigned by the Clinical Laboratory Improvement Amendments (CLIA) program to the laboratory director. Minimal field for US labs offering clinical tests. Optional field for international labs or US labs performing research tests. If pending renewal or record has not been updated, the expiration date may be in the past., Number: 37D0474681, Expiration date: 2022-10-19
CAP, Number: 2050201, Expiration date: 2021-12-10

Licenses

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.