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Results: 21 to 40 of 55

Tests names and labsConditionsGenes, analytes, and microbesMethods

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

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

HEREDITARY ATAXIAS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
11202
  • E Sequence analysis of select exons

Kallmann syndrome panel. 9-gene NGS panel.

Genologica Medica
Spain
179
  • C Sequence analysis of the entire coding region

Genital Abnormalities / Sex Development Disorders Panel

Genologica Medica
Spain
9549
  • C Sequence analysis of the entire coding region

Amelogenesis

Bioarray
Spain
1172
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Kallmann Syndrome Genetic Panel

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
2524
  • C Sequence analysis of the entire coding region

Congenital Hypotonia Xpanded Panel

GeneDx
United States
101423
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Custom XomeDx Slice – Differences of Sex Development (Proband Only)

GeneDx
United States
21112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prenatal Known Familial Mutation

GeneDx
United States
11716
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Custom XomeDxSlice (2-150 Genes, Proband Only)

GeneDx
United States
11718
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Premature Ovarian Failure Panel

GeneDx
United States
622
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypogonadotrophic Hypogonadism Panel

GeneDx
United States
533
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia Xpanded Panel

GeneDx
United States
1999
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypogonadotropic hypogonadism with or without anosmia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2424
  • C Sequence analysis of the entire coding region

Kallmann Syndrome & Hypogonadotropic Hypogonadism NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3439
  • C Sequence analysis of the entire coding region

PROK2 Single Gene

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

KALLMANN SYNDROME

Laboratorio de Genetica Clinica SL
Spain
66
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KALLLMAN SYNDROME (HYPOGONADOTROPIC HYPOGONADISM)

Laboratorio de Genetica Clinica SL
Spain
66
  • C Sequence analysis of the entire coding region

Kallmann syndrome

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

Results: 21 to 40 of 55

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.