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GTR Home > Laboratories > Molecular Diagnostic Laboratory

Molecular Diagnostic Laboratory

GTR Lab ID: 1070, Last updated:2023-09-25

Personnel

Conditions and tests

  • Angelman syndrome1 test
  • Autosomal recessive nonsyndromic hearing loss 1A1 test
  • Azorean disease1 test
  • Charcot-Marie-Tooth disease, type IA1 test
  • chronic recurrent pancreatitis1 test
  • Congenital bilateral aplasia of vas deferens from CFTR mutation1 test
  • Cystic fibrosis1 test
  • Disorder of cardiovascular system1 test
  • Disseminated bronchiectasis1 test
  • Fragile X syndrome1 test
  • Fragile X-associated tremor/ataxia syndrome1 test
  • Hemochromatosis type 11 test
  • Hereditary liability to pressure palsies1 test
  • Huntington disease1 test
  • Hypophosphatasia1 test
  • Kennedy disease1 test
  • Oculopharyngeal muscular dystrophy1 test
  • Prader-Willi syndrome1 test
  • Premature ovarian failure 11 test
  • Recurrent acute pancreatitis1 test
  • Spermatogenic failure, Y-linked, 21 test
  • Spinocerebellar ataxia 71 test
  • Spinocerebellar ataxia type 11 test
  • Spinocerebellar ataxia type 21 test
  • Spinocerebellar ataxia type 61 test
  • Spinocerebellar ataxia type 81 test
  • Steinert myotonic dystrophy syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously

List of certifications/licenses

Certifications

  • CAP, Number: 6690201, Expiration date: 2025-02-17

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.