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Results: 1 to 13 of 13

Tests names and labsConditionsGenes and analytesMethods

Hypogonadotropic hypogonadism

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypogonadotropic hypogonadism

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KALLMANN SYNDROME AND RELATED DISORDERS

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1616
  • C Sequence analysis of the entire coding region

Abnormal/Ambiguous Genitalia Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
8272
  • C Sequence analysis of the entire coding region

Hypogonadotropic Hypogonadism Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
1420
  • C Sequence analysis of the entire coding region

Hypogonadotropic hypogonadism 9 with or without anosmia (sequence analysis of NSMF gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

NSMF

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypogonadotropic Hypogonadism (HH) and Related Disorders NGS Panel

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

Endocrine Disorders: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
10857
  • C Sequence analysis of the entire coding region

Kallmann Syndrome NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
2713
  • 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 13 of 13

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.