U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 61 to 70 of 70

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Skeletal Dysplasias and Disorders Panel

Blueprint Genetics
Finland
1246
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniofacial Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
4744
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniosynostosis Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
3531
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

qGenEx Craniofacial Anomalies

Quantitative Genomic Medicine Laboratories, SL
Spain
135136
  • C Sequence analysis of the entire coding region

Craniosynostosis Panel

Blueprint Genetics
Finland
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TCF12 Single Gene

Fulgent Genetics
United States
261
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cancer RNA Fusion Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
2117
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Craniosynostosis syndromes Panel

CeGaT GmbH
Germany
2020
  • C Sequence analysis of the entire coding region

Hemato-oncology chromosomal microarray

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
2393
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Kallmann Syndrome

MGH Harvard Center for Reproductive Medicine Massachusetts General Hospital
United States
259
  • C Sequence analysis of the entire coding region

Results: 61 to 70 of 70

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.