U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

Results: 61 to 73 of 73

Tests names and labsConditionsGenes, analytes, and microbesMethods

FGFR-Related Craniosynostosis NGS Panel

Fulgent Genetics
United States
253
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypogonadotropic Hypogonadism (HH) and Related Disorders NGS Panel

Fulgent Genetics
United States
2213
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Complete Kallmann/IHH Evaluation

Athena Diagnostics
United States
1010
  • C Sequence analysis of the entire coding region

Anosmic Kallmann/IHH Evaluation

Athena Diagnostics
United States
77
  • C Sequence analysis of the entire coding region

Normosmic Kallmann/IHH Evaluation

Athena Diagnostics
United States
77
  • C Sequence analysis of the entire coding region

FGFR1 DNA Sequencing Test

Athena Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Kallmann syndrome

Synlab MVZ Humane Genetik M√ľnchen
Germany
22
  • 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

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kallmann Syndrome NGS Panel

Fulgent Genetics
United States
2819
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kallmann syndrome 2

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kallmann syndrome 2

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kallmann syndrome 2

Institute of Human Genetics Cologne University
Germany
11
  • C Sequence analysis of the entire coding region

Results: 61 to 73 of 73

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.