Filters

See more specimen types...

Other countries

Results: 1 to 8 of 8 (representing 7 labs)

Tests names and labsConditionsGenes and analytesMethods

Constitutional Cytogenomic Microarray Analysis

Clinical Cytogenomics Laboratory University of Washington
United States
261
  • D Deletion/duplication analysis

Craniosynostosis

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
6626
  • C Sequence analysis of the entire coding region

Kallmann Syndrome Panel

Blueprint Genetics
Finland
18
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Isolated Gonadotropin-Releasing Hormone Deficiency Panel

Invitae
United States
43
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Epilepsy NGS Panel

Fulgent Genetics
United States
3052447
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Identifying Causative Genes in Kallman Syndrome

Molecular Endocrinology Laboratory Augusta University
United States
11
  • C Sequence analysis of the entire coding region

Kallmann Syndrome

Harvard Reproductive Endocrine Science Center Massachusetts General Hospital
United States
214
  • C Sequence analysis of the entire coding region

Identifying Causative Genes in GnRH Deficiency

Molecular Endocrinology Laboratory Augusta University
United States
21
  • C Sequence analysis of the entire coding region

Results: 1 to 8 of 8

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.

Support Center