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Results: 21 to 28 of 28

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hartnup Disease (SLC6A19 Single Gene Test)

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

IMINOGLYCINURIA/ HYPERGLICINURIA

Laboratorio de Genetica Clinica SL
Spain
24
  • C Sequence analysis of the entire coding region

Single gene testing SLC6A20

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Single gene testing SLC36A2

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

SLC6A20 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SLC36A2 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SLC6A19 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 28 of 28

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.