U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

Results: 61 to 79 of 79

Tests names and labsConditionsGenes, analytes, and microbesMethods

Bardet-Biedl syndrome panel

Molecular Vision Laboratory
United States
3823
  • 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

Limb-Girdle Muscular Dystrophies Panel

CeGaT GmbH
Germany
2834
  • C Sequence analysis of the entire coding region

TRIM32

MGZ Medical Genetics Center
Germany
21
  • C Sequence analysis of the entire coding region

Limb girdle muscular dystrophy-Panel

MVZ Dr. Eberhard & Partner Dortmund
Germany
1918
  • C Sequence analysis of the entire coding region

Limb girdle muscular dystrophy 2H

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

TRIM32 Single Gene

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

Limb-Girdle Muscular Dystrophy NGS Panel

Fulgent Genetics
United States
5120
  • D Deletion/duplication analysis
  • 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

Congenital Hepatic Fibrosis NGS Panel

Fulgent Genetics
United States
4734
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinitis Pigmentosa NGS Panel

Fulgent Genetics
United States
329124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuromuscular NGS Panel

Fulgent Genetics
United States
259112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Diabetes-Obesity NGS Panel

Fulgent Genetics
United States
7356
  • 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

Bardet-Biedl Syndrome NGS Panel

Fulgent Genetics
United States
1216
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ciliopathies NGS Panel

Fulgent Genetics
United States
14197
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophies NGS Panel

Fulgent Genetics
United States
12542
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular dystrophy, limb-girdle, type 2H

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Sarcotubular myopathy

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Results: 61 to 79 of 79

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.