Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese families.

about

Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese families.

Item

http://www.wikidata.org/entity/Q49235433

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Prenatal diagnosis and genetic ...... I and II in Chinese families.

@en

Prenatal diagnosis and genetic ...... I and II in Chinese families.

@nl

type

Item

label

Prenatal diagnosis and genetic ...... I and II in Chinese families.

@en

Prenatal diagnosis and genetic ...... I and II in Chinese families.

@nl

prefLabel

Prenatal diagnosis and genetic ...... I and II in Chinese families.

@en

Prenatal diagnosis and genetic ...... I and II in Chinese families.

@nl

P1476

Prenatal diagnosis and genetic ...... I and II in Chinese families.

@en

P2093

Dong Wu

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

Hongdan Wang

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

Hongjian Liu

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

Li Wang

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

Liangjie Guo

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

Lingcao Ma

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

Litao Qin

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

Qiannan Guo

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

Shixiu Liao

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

Tao Li

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

P2860

SLUG (SNAI2) deletions in patients with Waardenburg disease

Waardenburg syndrome

Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium

PAX3 gene deletion detected by microarray analysis in a girl with hearing loss

Microphthalmia-associated transcription factor (MITF): multiplicity in structure, function, and regulation.

Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type II.

The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia.

Worldwide distribution of Waardenburg syndrome.

Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders.

Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics.

P304

172-178

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

P31

scholarly article

P356

10.3892/MMR.2017.7874

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

P433

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

P478

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

P577

2017-10-25T00:00:00Z

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

P698

29115496

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

P932

5780116

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