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GTR Home > Laboratories > Molecular Genetics Laboratory

Molecular Genetics Laboratory

GTR Lab ID: 53259, Last updated:2023-04-06


Conditions and tests

  • Amyotrophic lateral sclerosis type 11 test
  • Cystic fibrosis1 test
  • DiGeorge syndrome1 test
  • Fragile X syndrome1 test
  • Fragile X-associated tremor/ataxia syndrome1 test
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 11 test
  • Hemochromatosis type 2A1 test
  • Hereditary pancreatitis1 test
  • Hypokalemic periodic paralysis, type 11 test
  • Juvenile myopathy, encephalopathy, lactic acidosis AND stroke1 test
  • Leber optic atrophy1 test
  • Lynch syndrome1 test
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
  • MERRF syndrome1 test
  • Mitochondrial DNA-Associated Leigh Syndrome and NARP1 test
  • Mitochondrial trifunctional protein deficiency1 test
  • Premature ovarian failure 11 test
  • Spermatogenic failure, Y-linked, 21 test
  • Velocardiofacial syndrome1 test
  • X-linked ichthyosis with steryl-sulfatase deficiency1 test

List of services

  • This lab has no services.

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.