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Results: 1 to 20 of 57 (representing 45 labs)

Tests names and labsConditionsGenes and analytesMethods

Baby Genes Targeted Panel

Baby Genes Inc.
United States
8990
  • T Targeted variant analysis

Congenital adrenal hyperplasia

Genomic Engenharia Molecular
Brazil
11
  • E Sequence analysis of select exons

Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency

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

Congenital Adrenal Hyperplasia due to 21-Hydroxylase deficiency

Molecular Genetics and Cytogenetics, Clinical Laboratory Service Faculty of Medicine, Pontificia Universidad Católica de Chile
Chile
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia (CAH)

Center for Genetics at Saint Francis Saint Francis Hospital
United States
11
  • C Sequence analysis of the entire coding region

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
328300
  • C Sequence analysis of the entire coding region

CYP21A2. Complete sequencing

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

CYP21A2. MLPA testing

Instituto de Medicina Genomica
Spain
11
  • D Deletion/duplication analysis

Congenital Adrenal Hyperplasia due to 21-hydroxylase deficiency via the CYP21A2 Gene

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

CYP21A2 target mutation analysis

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
31
  • X Mutation scanning of select exons
  • E Sequence analysis of select exons

CYP21A2 gene Sequencing

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
31
  • C Sequence analysis of the entire coding region

Ashkenazi Jewish diseases

Asper Biogene Asper Biogene LLC
Estonia
4337
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CONGENITAL ADRENAL HYPERPLASIA (11-BETA-HYDROXYLASE DEFICIENCY)

Laboratorio de Genetica Clinica SL
Spain
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CYP21A2 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
52
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia due to 21-Beta-Hydroxylase Deficiency, Sequencing CYP21A2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Adrenal hyperplasia due to 21-Hydroxylase deficiency

LifeLabs Genetics
Canada
11
  • D Deletion/duplication analysis
  • 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

CarrierMap

Recombine
United States
302301
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

21-hydroxylase deficiency (sequence analysis of CYP21A2 gene)

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

Results: 1 to 20 of 57

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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