Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V. - Test2 - elhamkhani - TriplyDB

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

http://www.wikidata.org/entity/Q34973809

about

Clinical and Molecular Characterization of Osteogenesis Imperfecta Type V.IFITMs restrict the replication of multiple pathogenic viruses IFITM5 mutations and osteogenesis imperfecta.Novel mutations in the SEC24D gene in Chinese families with autosomal recessive osteogenesis imperfecta.

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P2860

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

http://www.wikidata.org/entity/Q34973809

description

2013 nî lūn-bûn

@nan

2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

name

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@ast

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@en

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@nl

type

label

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@ast

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@en

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@nl

prefLabel

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@ast

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@en

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@nl

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P356

JOURNAL.PONE.0072337

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P1476

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

@en

P2093

Chang-Qing Zhang

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

Jin-Wei He

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Mei Li

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

Wen-Zhen Fu

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

Zeng Zhang

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

Zhen-Lin Zhang

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Exome sequencing identifies ZNF644 mutations in high myopia

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The novel zinc finger-containing transcription factor osterix is required for osteoblast differentiation and bone formation

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Genetic heterogeneity in osteogenesis imperfecta.

Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta

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Phenotypic variability of osteogenesis imperfecta type V caused by an IFITM5 mutation

Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta

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e72337

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scholarly article

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10.1371/JOURNAL.PONE.0072337

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8

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8

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2013-08-20T00:00:00Z

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256102667

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23977282

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osteogenesis imperfecta

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3748067

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