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Results: 181 to 195 of 195

Tests names and labsConditionsGenes, analytes, and microbesMethods

Nuclear encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
37302
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia (including hypotrichosis and hypoplastic hair) Panel

CeGaT GmbH
Germany
2955
  • C Sequence analysis of the entire coding region

Mitochondrial Encephalopathy

MGZ Medical Genetics Center
Germany
6131
  • C Sequence analysis of the entire coding region

Mitochondrial Hepato(encephalo)pathy and Phenocopies

MGZ Medical Genetics Center
Germany
615
  • C Sequence analysis of the entire coding region

Complex III Defect

MGZ Medical Genetics Center
Germany
35
  • C Sequence analysis of the entire coding region

Mitochondrial Diseases

MGZ Medical Genetics Center
Germany
6168
  • C Sequence analysis of the entire coding region

Mitochondrial Diseases (mtDNA and 217 nuclear genes)

Asper Biogene Asper Biogene LLC
Estonia
89210
  • C Sequence analysis of the entire coding region

BCS1L Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leigh Syndrome

MGZ Medical Genetics Center
Germany
323
  • 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

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • 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

Leigh Syndrome (nuclear DNA mutation)

MGZ Medical Genetics Center
Germany
125
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial Respiratory Chain Complex III Deficiency, BCS1L-Related

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

Results: 181 to 195 of 195

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.