U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

Results: 21 to 31 of 31

Tests names and labsConditionsGenes, analytes, and microbesMethods

Leber optic atrophy (sequence analysis of MTND4L gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Mitochondrial Diseases Panel (Nuclear and Mitochondrial DNA)

Mendelics
Brazil
1169
  • C Sequence analysis of the entire coding region

Mitochondrial Disorders Panel

Dhiti Omics Technologies Private Ltd
India
2837
  • C Sequence analysis of the entire coding region

Rapid MitoGenome Seq + Del

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoGenome Seq + Del

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Maternal MitoGenome Seq + Del

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
137
  • C Sequence analysis of the entire coding region

Common 29 mtDNA Variant Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
932
  • T Targeted variant analysis

MT-ND4L

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

Mitochondrial Genome NGS Panel

Fulgent Genetics
United States
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
372283
  • C Sequence analysis of the entire coding region

mtDNA encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
1137
  • C Sequence analysis of the entire coding region

Results: 21 to 31 of 31

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.