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Results: 81 to 96 of 96

Tests names and labsConditionsGenes, analytes, and microbesMethods

Metabolic Epilepsy Panel

Blueprint Genetics
Finland
841
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism Panel

Blueprint Genetics
Finland
14434
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Movement Disorders Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
492
  • C Sequence analysis of the entire coding region

Infantile Epilepsy

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
260
  • C Sequence analysis of the entire coding region

Epilepsy/Seizure

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
598
  • C Sequence analysis of the entire coding region

Dystonia

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
477
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing QDPR

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Hyperphenylalaninemia Panel

CeGaT GmbH
Germany
34
  • C Sequence analysis of the entire coding region

Metabolic Epilepsy Panel

CeGaT GmbH
Germany
337
  • C Sequence analysis of the entire coding region

QDPR Single Gene

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

Hyperphenylalaninemia, BH4-deficient, C (QDPR)

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
11
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • 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

Lysosomal Disorders NGS Panel

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

BH4-Deficient Hyperphenylalaninemia C

Department of Clinical Genetics Copenhagen University Hospital, Rigshospitalet
Denmark
11
  • C Sequence analysis of the entire coding region

Results: 81 to 96 of 96

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.