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Results: 21 to 29 of 29

Tests names and labsConditionsGenes, analytes, and microbesMethods

LTBP2 single gene sequencing

Molecular Vision Laboratory
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ectopia Lentis NGS Panel

Fulgent Genetics
United States
4915
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Micromelic Dysplasia NGS Panel

Fulgent Genetics
United States
14024
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Weill-Marchesani Syndrome: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
44
  • C Sequence analysis of the entire coding region

LTBP2 Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glaucoma NGS Panel

Fulgent Genetics
United States
6826
  • 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

LTBP2-Related Weill-Marchesani Syndrome

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

Results: 21 to 29 of 29

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.