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Results: 1 to 20 of 29

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

Baby Genes Targeted Panel

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

CEN4GEN rapid supplemental newborn genetic screen: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
199
  • C Sequence analysis of the entire coding region

CEN4GEN rapid pan-ethnic carrier screen: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1104
  • C Sequence analysis of the entire coding region

Congenital Hypothyroidism Deletion/Duplication Panel

Genetic Services Laboratory University of Chicago
United States
1122
  • D Deletion/duplication analysis

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
328300
  • 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 SLC5A5/NIS Gene

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

Congenital hypothyroidism: gene sequencing panel (RAPID testing)

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
19
  • C Sequence analysis of the entire coding region

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

Thyroid dyshormonogenesis 1: Full gene sequencing (Rapid testing)

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • 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
  • C Sequence analysis of the entire coding region

Hypothyroidism and Thyroid Hormone Resistance

Asper Biogene Asper Biogene LLC
Estonia
2921
  • 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 1 , Sequencing SLC5A5 Gene

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

Congenital Hypothyroidism Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
1122
  • C Sequence analysis of the entire coding region

Hypothyroidism and Resistance to Thyroid Hormone Panel

Blueprint Genetics
Finland
217
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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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