GTR Home > Laboratories > Molecular Diagnostic Laboratory

Molecular Diagnostic Laboratory

GTR Lab ID: 53259, Last updated:2016-04-05


Conditions and tests

  • 1q21.1 recurrent microdeletion1 test
  • Amyotrophic lateral sclerosis type 11 test
  • Arrhythmogenic right ventricular cardiomyopathy, type 51 test
  • ATR-X syndrome1 test
  • Cystic fibrosis1 test
  • Deafness, autosomal dominant 3a1 test
  • Deafness, autosomal recessive 1A1 test
  • Deafness, nonsyndromic sensorineural, mitochondrial1 test
  • DiGeorge sequence1 test
  • Dystonia 11 test
  • Fragile X syndrome1 test
  • Fragile X tremor/ataxia syndrome1 test
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis1 test
  • Glaucoma, congenital1 test
  • Hemochromatosis type 2A1 test
  • Hereditary pancreatitis1 test
  • Hypokalemic periodic paralysis 11 test
  • Juvenile myopathy, encephalopathy, lactic acidosis AND stroke1 test
  • Leber's optic atrophy1 test
  • Lynch syndrome1 test
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
  • Mitochondrial DNA-Associated Leigh Syndrome and NARP1 test
  • Mitochondrial trifunctional protein deficiency1 test
  • Myoclonus with epilepsy with ragged red fibers1 test
  • Premature ovarian failure 11 test
  • Shprintzen syndrome1 test
  • Spermatogenic failure, Y-linked 21 test
  • Williams syndrome1 test
  • Williams-Beuren region duplication 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.