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Results: 121 to 133 of 133

Tests names and labsConditionsGenes, analytes, and microbesMethods

Peroxisomal Disorders Panel

CeGaT GmbH
Germany
216
  • C Sequence analysis of the entire coding region

Leukodystrophy / Leukencephalopathy and differential diagnoses Panel

CeGaT GmbH
Germany
69175
  • C Sequence analysis of the entire coding region

Peroxisomal Disorder Panel

CeGaT GmbH
Germany
216
  • C Sequence analysis of the entire coding region

Peroxisome disorders: Zellweger Spectrum and Related Single Enzyme Defects

Braverman Laboratory Research Institute of the McGill University Health Center
Canada
120
  • A Analyte
  • I Immunohistochemistry
  • C Sequence analysis of the entire coding region

PEX16 Single Gene

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

Cholestasis NGS Panel

Fulgent Genetics
United States
12166
  • 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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Zellweger Syndrome NGS Panel

Fulgent Genetics
United States
2012
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Peroxisomal NGS Panel

Fulgent Genetics
United States
7621
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lysosomal Disorders NGS Panel

Fulgent Genetics
United States
186106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Zellweger Syndrome Spectrum

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
113
  • A Analyte
  • E Enzyme assay
  • X Protein expression
  • C Sequence analysis of the entire coding region

Results: 121 to 133 of 133

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.