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Results: 1 to 17 of 17

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 Newborn Screening Panel

Baby Genes Inc.
United States
6581
  • T Targeted variant analysis

Thyroid dyshormonogenesis 2A

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

Congenital Hypothyroidism (Thyroid Dyshormonogenesis) via the TPO Gene

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

Congenital Hypothyroidism and Thyroid Hormone Resistance Nextgen Sequencing (NGS) Panel

PreventionGenetics
United States
2218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

TPO. Complete sequencing

Instituto de Medicina Genomica
Spain
21
  • 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

Familial thyroid dyshormonogenesis type 2A

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

TPO

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

Thyroid dyshormonogenesis 2A (sequence analysis of TPO gene)

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

Hypothyroidism, Congenital: TPO gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Thyroid dyshormonogenesis 2A

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Thyroid dyshormonogenesis 2A

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

TPO mutation analysis

DNA Diagnostics Laboratory Academic Medical Centre, University of Amsterdam
Netherlands
11
  • L Linkage analysis
  • C Sequence analysis of the entire coding region

TPO

Innovagenomics Innovagenomics S.L
Spain
11
  • S Mutation scanning of the entire coding region
  • C Sequence analysis of the entire coding region

Results: 1 to 17 of 17

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.