The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.

about

The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.

Item

http://www.wikidata.org/entity/Q54960339

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh

2018年學術文章

@zh-hant

name

The genetic characteristics of ...... reening of 21 candidate genes.

@en

The genetic characteristics of ...... reening of 21 candidate genes.

@nl

type

Item

label

The genetic characteristics of ...... reening of 21 candidate genes.

@en

The genetic characteristics of ...... reening of 21 candidate genes.

@nl

prefLabel

The genetic characteristics of ...... reening of 21 candidate genes.

@en

The genetic characteristics of ...... reening of 21 candidate genes.

@nl

P1476

The genetic characteristics of ...... reening of 21 candidate genes.

@en

P2093

Bing Han

http://www.w3.org/2001/XMLSchema#string

Chang-Yi Yang

http://www.w3.org/2001/XMLSchema#string

Cui-Cui Guo

http://www.w3.org/2001/XMLSchema#string

Feng Sun

http://www.w3.org/2001/XMLSchema#string

Gang Chen

http://www.w3.org/2001/XMLSchema#string

Guan-Qi Gao

http://www.w3.org/2001/XMLSchema#string

Huai-Dong Song

http://www.w3.org/2001/XMLSchema#string

Jun-Xiu Zhang

http://www.w3.org/2001/XMLSchema#string

Ke-Yi Song

http://www.w3.org/2001/XMLSchema#string

Le-Le Zhang

http://www.w3.org/2001/XMLSchema#string

P2860

Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism

Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor beta

Genetic causes of congenital hypothyroidism due to dyshormonogenesis

High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis

Congenital hypothyroidism.

European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia.

Functional zebrafish studies based on human genotyping point to netrin-1 as a link between aberrant cardiovascular development and thyroid dysgenesis

Genetics of congenital hypothyroidism

P304

623-633

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1530/EJE-17-1017

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

178

http://www.w3.org/2001/XMLSchema#string

P577

2018-04-12T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29650690

http://www.w3.org/2001/XMLSchema#string

P932

5958289

http://www.w3.org/2001/XMLSchema#string