Article

Clinical and molecular characteristics of congenital hypothyroidism with DUOX2 mutations

2013-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: b9abd7f4-cf9a-5431-8ceb-b0b5b3547754
DOI: 10.1186/1687-9856-2013-s1-o54
PMCID: PMC3849924

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Clinical and molecular characteristics of congenital hypothyroidism with DUOX2 mutationsDOI 10.1186/1687-9856-2013-s1-o54Read

Mutation Screening of DUOX2 Gene in Children with Congenital HypothyroidismSemantic proximity Read

Molecular and Clinical Features of Congenital Hypothyroidism Due to Multiple DUOX2 Variants.Semantic proximity Read

The Prevalence, Clinical, and Molecular Characteristics of Congenital Hypothyroidism Caused by DUOX2 Mutations: A Population-Based Cohort Study in Guangzhou.Semantic proximity Read

DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population.Semantic proximity Read

[DUOX2 mutations in children with congenital hypothyroidism].Semantic proximity Read

DUOX2 Mutations Are Associated With Congenital Hypothyroidism With Ectopic Thyroid Gland.Semantic proximity Read

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism.Semantic proximity Read

Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases.Semantic proximity Read

Combining whole-exome sequencing with clinical data for genotype–phenotype correlation in patients with congenital hypothyroidism that include the DUOX2 gene variationSemantic proximity Read

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism.Semantic proximity Read

Heterozygous Mutations of the DUOXA2 and DUOX2 Genes in Dizygotic Twins with Congenital Hypothyroidism.Semantic proximity Read

Patients with Thyroid Dyshormonogenesis and DUOX2 Variants: Molecular and Clinical Description and Genotype-Phenotype Correlation.Semantic proximity Read