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GTR Home > Laboratories > Genetics Laboratory

Genetics Laboratory

  • Genetics Laboratory
  • University of Oklahoma Health Sciences Center (OUHSC)
  • Department: Pediatrics
  • 1122 NE 13 Street, Room 1400
  • Oklahoma City, Oklahoma, United States 73117
  • Phone: 4052713589
    Fax: 4052717117
    Email: sherrill.marble@ouhealth.com
  • Website: http://www.genetics.ouhsc.edu/
  • Affiliated with:
    • Sherrill Gerding

GTR Lab ID: 1234, Last updated:2022-06-01

Personnel

  • Director: Young Mi Kim, PhD, ABMG, FACMG, DABMG, Lab Director
    Phone: 4052713581
    Fax: 4052714869
    Email: Young-Kim@ouhsc.edu
  • Director: Shibo Li, MD, ABMG, FACMG, DABMG, Lab Director
    Phone: 405-271-3590
    Fax: 405-271-7117
    Email: shibo-li@ouhsc.edu
  • Director: Hui Pang, PhD, MD, ABP, FACMG, Lab Director
    Phone: 405-271-4401
    Fax: 405-271-8697
    Email: Hui-Pang@ouhsc.edu
  • Sherrill Gerding, BS, Administrator
    Phone: 405-271-3589
    Fax: 405-271-4869
    Email: sherrill.marble@ouhealth.com

Conditions and tests

  • Adams-Oliver syndrome1 test
  • Adams-Oliver syndrome 11 test
  • Adams-Oliver syndrome 21 test
  • Adams-Oliver syndrome 31 test
  • Adams-Oliver syndrome 41 test
  • Angelman syndrome1 test
  • Autosomal dominant nonsyndromic hearing loss 3A1 test
  • Bartter disease type 11 test
  • Bartter disease type 21 test
  • Bartter disease type 31 test
  • Bartter disease type 4B1 test
  • Bartter disease type 51 test
  • Bernard Soulier syndrome1 test
  • Biotinidase deficiency1 test
  • Breast-ovarian cancer, familial, susceptibility to, 11 test
  • Breast-ovarian cancer, familial, susceptibility to, 21 test
  • Cardiofaciocutaneous syndrome 11 test
  • CHARGE association1 test
  • chronic recurrent pancreatitis1 test
  • Cockayne syndrome type 11 test
  • Costello syndrome1 test
  • Cystic fibrosis1 test
  • Deficiency of butyryl-CoA dehydrogenase1 test
  • Disorder of ketone body transport1 test
  • Disorder of lysosomal-related organelles1 test
  • Disorder of sexual differentiation1 test
  • Ehlers-Danlos syndrome, musculocontractural type1 test
  • Familial adenomatous polyposis 11 test
  • Familial adenomatous polyposis 21 test
  • Familial hypercholesterolemia2 tests
  • Familial hyperinsulinism1 test
  • Fragile X syndrome1 test
  • Galactosemia1 test
  • Generalized juvenile polyposis/juvenile polyposis coli1 test
  • Genetic hypoparathyroidism1 test
  • Glutaric aciduria, type 11 test
  • Hereditary cancer-predisposing syndrome1 test
  • Hereditary leiomyomatosis and renal cell cancer1 test
  • Hereditary nonpolyposis colon cancer1 test
  • Huntington disease1 test
  • Hyperinsulinemic hypoglycemia1 test
  • Hypertriglyceridemia, familial1 test
  • Hypertrophic cardiomyopathy 11 test
  • Hypogonadotropic hypogonadism1 test
  • Hypogonadotropic hypogonadism 3 with or without anosmia1 test
  • Hypophosphatemic rickets1 test
  • Hypopituitarism, congenital, with central diabetes insipidus1 test
  • Infantile epilepsy syndrome1 test
  • Isovaleric acidemia, type I1 test
  • Kabuki syndrome 11 test
  • Legius syndrome1 test
  • Li-Fraumeni syndrome1 test
  • Liddle syndrome1 test
  • Long QT syndrome1 test
  • Lynch syndrome1 test
  • Lynch syndrome 11 test
  • Macrocephaly, benign familial1 test
  • Malignant neoplasm of endocrine gland1 test
  • Marfan syndrome1 test
  • Marinesco-Sj√∂gren syndrome1 test
  • Maturity onset diabetes mellitus in young1 test
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
  • Melanoma, cutaneous malignant, susceptibility to, 21 test
  • Monogenic Non-Syndromic Obesity, Autosomal Recessive1 test
  • Multiple congenital exostosis1 test
  • Multiple endocrine neoplasia, type 11 test
  • Myotonic dystrophy1 test
  • Neuroendocrine neoplasm1 test
  • Neurofibromatosis, type 11 test
  • Noonan syndrome 31 test
  • Osteogenesis imperfecta1 test
  • Osteopetrosis with renal tubular acidosis1 test
  • Overlapping connective tissue disease1 test
  • Papillary renal cell carcinoma1 test
  • Paragangliomas 11 test
  • Paragangliomas 21 test
  • Paragangliomas 31 test
  • Paragangliomas 41 test
  • Periodic fever syndrome1 test
  • Prader-Willi syndrome1 test
  • PTEN hamartoma tumor syndrome1 test
  • Rett syndrome1 test
  • Severe short stature1 test
  • Sotos syndrome 11 test
  • Spinal muscular atrophy1 test
  • Syndromic hypothyroidism1 test
  • Thrombocytopenia, X-linked, with or without dyserythropoietic anemia1 test
  • Von Hippel-Lindau syndrome1 test
  • Williams syndrome1 test
  • Wilson disease1 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
  • Custom microarray analysis
  • DNA Banking
  • Marker Chromosome Identification
  • Maternal cell contamination study (MCC)
  • Uniparental Disomy (UPD) Testing

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 37D0967945, Expiration date: 2023-07-17
  • CAP, Number: 2038704, Expiration date: 2022-06-27

Participation in external programs

Standardization programs

  • Locus-specific Databases
  • Mutation-specific Databases

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.