U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

Results: 41 to 51 of 51

Tests names and labsConditionsGenes, analytes, and microbesMethods

Microphthalmia, Anophthalmia, and Coloboma Panel NGS Panel

Fulgent Genetics
United States
24478
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniometaphyseal Dysplasia, Panel Massive Sequencing (NGS) ANKH, GJA1 Genes

Reference Laboratory Genetics
Spain
22
  • C Sequence analysis of the entire coding region

Craniometaphyseal Dysplasia , Sequencing GJA1 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Skeletal dysplasia with increased bone density Panel

CeGaT GmbH
Germany
2628
  • C Sequence analysis of the entire coding region

Single gene testing GJA1

CeGaT GmbH
Germany
61
  • C Sequence analysis of the entire coding region

GJA1 Single Gene

Fulgent Genetics
United States
61
  • 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 heart defects panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
6934
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • 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

Genetic and Functional Analysis of Craniometaphyseal Dysplasia

Center for Regenerative Medicine and Skeletal Development University of Connecticut Health Center
United States
11
  • C Sequence analysis of the entire coding region

Results: 41 to 51 of 51

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.