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Results: 1 to 18 of 18

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Thyroid dyshormonogenesis type 5

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

Congenital Hypothyroidism and Thyroid Hormone Resistance Sequencing Panel with CNV Detection

PreventionGenetics
United States
3226
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Congenital Hypothyroidism (Thyroid Dyshormonogenesis) via the DUOXA2 Gene

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

Congenital Hypothyroidism , Panel Massive Sequencing 20 Genes

Reference Laboratory Genetics
Spain
2419
  • C Sequence analysis of the entire coding region

Familial Thyroid Dyshormogenesis , Panel Massive Sequencing (NGS) 10 Genes

Reference Laboratory Genetics
Spain
1410
  • C Sequence analysis of the entire coding region

CONGENITAL HYPOTHYROIDISM – NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
1414
  • C Sequence analysis of the entire coding region

Thyroid Dyshormonogenesis

Asper Biogene Asper Biogene LLC
Estonia
76
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypothyroidism and Thyroid Hormone Resistance

Asper Biogene Asper Biogene LLC
Estonia
2921
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CONGENITAL HYPOTHYROIDISM

Laboratorio de Genetica Clinica SL
Spain
88
  • C Sequence analysis of the entire coding region

Familial Thyroid Dyshormogenesis Type 5 , Sequencing DUOXA2 Gene

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

DUOXA1

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

Thyroid dyshormonogenesis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1210
  • C Sequence analysis of the entire coding region

CONGENITAL HYPOTHYROIDISM

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1922
  • C Sequence analysis of the entire coding region

Single gene testing DUOXA2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

DUOXA2

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

DUOXA2 mutation analysis

Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam
Netherlands
11
  • C Sequence analysis of the entire coding region

Results: 1 to 18 of 18

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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