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Results: 1 to 20 of 22 (representing 16 labs)

Tests names and labsConditionsGenes and analytesMethods

Kallmann syndrome type 4

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

PROK2 Gene Sequencing

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
11
  • C Sequence analysis of the entire coding region

Disorders of Sex Development Sequencing Panel

PreventionGenetics
United States
6469
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Disorders of Sex Development and Infertility Sequencing Panel

PreventionGenetics
United States
8696
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Male Infertility Sequencing Panel

PreventionGenetics
United States
7380
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Female Infertility Sequencing Panel

PreventionGenetics
United States
7683
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypogonadotropic Hypogonadism/Kallmann Syndrome via the PROK2 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PROK2. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Kallmann syndrome

Labor Dr. Wisplinghoff
Germany
44
  • C Sequence analysis of the entire coding region

Hypogonadotropic Hypogonadism/Kallmann Syndrome Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
1911
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kallmann syndrome/gonadotropin-releasing hormone deficiency panel

LifeLabs Genetics
Canada
1111
  • 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

Kallmann syndrome

bio.logis Center for Human Genetics
Germany
66
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypogonadotropic hypogonadism 4 with or without anosmia

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Hypogonadotropic hypogonadism 4 with or without anosmia (sequence analysis of PROK2 gene)

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

Complete Kallmann/IHH Evaluation

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

PROK2 DNA Sequencing Test

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

Anosmic Kallmann/IHH Evaluation

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

Normosmic Kallmann/IHH Evaluation

Athena Diagnostics Inc
United States
77
  • 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

Results: 1 to 20 of 22

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.

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