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Results: 81 to 85 of 85

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hyperoxaluria, primary I

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary Hyperoxaluria (Type 1, Type 2, Type 3) Genetic Testing

Rare Kidney Stone Consortium And The Mayo Clinic Hyperoxaluria Center Mayo Clinic
United States
43
  • C Sequence analysis of the entire coding region

Hyperoxaluria, Primary, Type 1

Institute of Human Genetics Cologne University
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary hyperoxaluria, type I

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperoxaluria, primary, type 1 (AGXT gene)

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
11
  • A Analyte
  • E Enzyme assay
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 81 to 85 of 85

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.