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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Peters-plus syndrome (frequent mutations of B3GALTL gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

GeneSeq® Metabolic: Lysosomal Storage Disorders Panel

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
159
  • C Sequence analysis of the entire coding region

Metabolic Diseases Panel

CGC Genetics Unilabs
Portugal
1837
  • C Sequence analysis of the entire coding region

Parkinson's and movement disorders panel_v.2.0

CGC Genetics Unilabs
Portugal
1256
  • C Sequence analysis of the entire coding region

Ataxia Xpanded Panel

GeneDx
United States
1999
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

VPS16 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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.