Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.

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Chromosomal and subchromosomal anomalies associated to small for gestational age fetuses with no additional structural anomalies.Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation: A case report.

P2860

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P2860

Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.

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http://www.wikidata.org/entity/Q38970186

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2017 nî lūn-bûn

@nan

2017年の論文

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2017年学术文章

@wuu

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

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2017年學術文章

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2017年學術文章

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name

Prenatal diagnosis of Duchenne ...... amilies with dystrophinopathy.

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type

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label

Prenatal diagnosis of Duchenne ...... amilies with dystrophinopathy.

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Prenatal diagnosis of Duchenne ...... amilies with dystrophinopathy.

@en

P1476

Prenatal diagnosis of Duchenne ...... families with dystrophinopathy

@en

P2093

Bing Xiao

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Lei Wang

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

Wei Wei

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

Weiping Ye

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

Wenting Jiang

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

Xiaoqing Liu

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

Xing Ji

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

Yan Xu

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

Yingwei Chen

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P2860

Population frequencies of inherited neuromuscular diseases--a world survey

DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations

MLPA-based genotype-phenotype analysis in 1053 Chinese patients with DMD/BMD.

Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy.

Whole dystrophin gene analysis by next-generation sequencing: a comprehensive genetic diagnosis of Duchenne and Becker muscular dystrophy.

The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.

Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.

The structural and functional diversity of dystrophin.

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.

A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male.

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356-364

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P31

scholarly article

P356

10.1002/PD.5019

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P433

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

P478

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Huanhuan Wang

P577

2017-03-06T00:00:00Z

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P698

28181689

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Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.

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P2860

P2860

Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698