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Results: 61 to 66 of 66

Tests names and labsConditionsGenes, analytes, and microbesMethods

Nuclear-Mito NGS Panel

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

Lactic Acidosis-Pyruvate NGS Panel

Fulgent Genetics
United States
9569
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Fatal Infantile Cardioencephalomyopathy due to Cytochrome c Oxidase Deficiency

MGZ Medical Genetics Center
Germany
11
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
13098
  • C Sequence analysis of the entire coding region

Fatal Infantile Cardioencephalomyopathy due to Cytochrome c Oxidase Deficiency

John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
United States
11
  • C Sequence analysis of the entire coding region

Results: 61 to 66 of 66

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.