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Results: 101 to 109 of 109

Tests names and labsConditionsGenes, analytes, and microbesMethods

NR0B1 Single Gene

Fulgent Genetics
United States
21
  • 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

NR0B1 (Adrenal Hypoplasia Congenita) DNA Sequencing Test

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

Primary Adrenal Insufficiency Evaluation

Athena Diagnostics
United States
33
  • 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

Kallmann Syndrome NGS Panel

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

Disorders of Sex Development

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
188
  • C Sequence analysis of the entire coding region

Hypogonadotrophic Hypogonadism

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
130
  • C Sequence analysis of the entire coding region

Kallmann Syndrome

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

Results: 101 to 109 of 109

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.