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GTR Home > Laboratories > Molecular Diagnosis Centre

Molecular Diagnosis Centre

GTR Lab ID: 320477, Last updated:2022-06-24
Annual Review past due read more

Personnel

Conditions and tests

  • Angelman syndrome1 test
  • Autosomal recessive nonsyndromic hearing loss 1A1 test
  • Hemochromatosis type 11 test
  • Hereditary hearing loss and deafness1 test
  • Leber optic atrophy1 test
  • Mitochondrial non-syndromic sensorineural hearing loss1 test
  • MTHFR THERMOLABILE POLYMORPHISM1 test
  • MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA1 test
  • MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB1 test
  • Prader-Willi syndrome1 test
  • Spermatogenic failure, Y-linked, 21 test
  • Spondyloarthropathy, susceptibility to1 test
  • Thrombophilia1 test
  • Thrombophilia due to activated protein C resistance1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Sequence Analysis
  • Carrier testing

List of certifications/licenses

Certifications

  • CAP, Number: 3010701, Expiration date: 2021-03-31
  • ISO 15189 - SAC-SINGLAS, Number: -, Expiration date: 2021-08-01
  • OHSAS 18001, Number: -, Expiration date: 2020-12-29

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.