Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

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Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome Toward an orofacial gene regulatory network.

P2860

Q24645286-0F66185D-BDAC-40D4-8D88-40EA7E5E1121 Q36586034-38184072-E691-450F-A79F-68E64F50A89E

P2860

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

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http://www.wikidata.org/entity/Q52006307

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2006 nî lūn-bûn

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2006年の論文

@ja

2006年学术文章

@wuu

2006年学术文章

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2006年学术文章

@zh-cn

2006年学术文章

@zh-hans

2006年学术文章

@zh-my

2006年学术文章

@zh-sg

2006年學術文章

@yue

2006年學術文章

@zh-hant

name

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

@en

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

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type

Item

label

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

@en

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

@nl

prefLabel

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

@en

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

@nl

P1476

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

@en

P2093

L Liu

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S Li

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

W Tang

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

W Tian

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

X Chen

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

X Du

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

X Li

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

X Zheng

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

Y Lin

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

Y Tang

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

P2860

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Analysis of functional domains of interferon regulatory factor 7 and its association with IRF-3

Interferon regulatory factors: the next generation.

Novel mutation of the initiation codon of PAX9 causes oligodontia.

Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene.

Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion.

Conserved transactivation domain shared by interferon regulatory factors and Smad morphogens.

Two missense mutations in the IRF6 gene in two Japanese families with Van der Woude syndrome.

A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndrome.

Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.

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937-940

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scholarly article

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10.1177/154405910608501013

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English

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2006-10-01T00:00:00Z

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16998136

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Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

about

P2860

P2860

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698