Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity.

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Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity.

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

@zh-cn

2014年学术文章

@zh-hans

2014年学术文章

@zh-my

2014年学术文章

@zh-sg

2014年學術文章

@yue

2014年學術文章

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Identification of a novel SHOX ...... h isolated Madelung deformity.

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Identification of a novel SHOX ...... h isolated Madelung deformity.

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Item

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Identification of a novel SHOX ...... h isolated Madelung deformity.

@en

Identification of a novel SHOX ...... h isolated Madelung deformity.

@nl

prefLabel

Identification of a novel SHOX ...... h isolated Madelung deformity.

@en

Identification of a novel SHOX ...... h isolated Madelung deformity.

@nl

P1476

Identification of a novel SHOX ...... h isolated Madelung deformity.

@en

P2093

Desheng Liang

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

Haoxian Li

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

Libin Mei

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

Lingqian Wu

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

Qian Pan

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

Yanru Huang

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P2860

PHOG, a candidate gene for involvement in the short stature of Turner syndrome

SHOX point mutations in dyschondrosteosis

Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOX.

Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood.

Otto W. Madelung and the recognition of Madelung's deformity.

Madelung deformity in a girl with a novel and de novo mutation in theGNASgene

P2888

s12041-014-0419-3

P304

809-812

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P31

scholarly article

P356

10.1007/S12041-014-0419-3

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P433

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

P478

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

P577

2014-12-01T00:00:00Z

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P5875

270657932

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P698

25572239

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