U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

Results: 21 to 33 of 33

Tests names and labsConditionsGenes, analytes, and microbesMethods

Retinitis Pigmentosa (Complet Panel) , Panel Massive Sequencing (NGS) 57 Genes

Reference Laboratory Genetics
Spain
5757
  • C Sequence analysis of the entire coding region

Autosomal Dominant Retinitis Pigmentosa, Panel Massive Sequencing (NGS) 27 Genes

Reference Laboratory Genetics
Spain
2627
  • C Sequence analysis of the entire coding region

Macular Degeneration NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
2624
  • C Sequence analysis of the entire coding region

Retinitis Pigmentosa NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
10392
  • C Sequence analysis of the entire coding region

Eye diseases comprehensive panel

Asper Biogene Asper Biogene LLC
Estonia
367291
  • 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

Retinitis pigmentosa, autosomal dominant and X-linked Panel

CeGaT GmbH
Germany
2430
  • C Sequence analysis of the entire coding region

GUCA1B Single Gene

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

Autosomal Dominant Retinitis Pigmentosa

Asper Biogene Asper Biogene LLC
Estonia
2526
  • 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

Retinitis Pigmentosa NGS Panel

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

Autosomal Recessive Retinitis Pigmentosa

Asper Biogene Asper Biogene LLC
Estonia
5756
  • 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

Results: 21 to 33 of 33

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.