Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting.

about

Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting.

Item

http://www.wikidata.org/entity/Q53673157

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年学术文章

@wuu

2014年学术文章

@zh

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

@zh-hant

name

Novel Mutations in the IRF6 Ge ...... ients With Orofacial Clefting.

@en

Novel Mutations in the IRF6 Ge ...... ients With Orofacial Clefting.

@nl

type

Item

label

Novel Mutations in the IRF6 Ge ...... ients With Orofacial Clefting.

@en

Novel Mutations in the IRF6 Ge ...... ients With Orofacial Clefting.

@nl

prefLabel

Novel Mutations in the IRF6 Ge ...... ients With Orofacial Clefting.

@en

Novel Mutations in the IRF6 Ge ...... ients With Orofacial Clefting.

@nl

P1476

Novel Mutations in the IRF6 Ge ...... ients With Orofacial Clefting.

@en

P2093

Agnieszka Charzewska

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

Dorota Hoffman-Zacharska

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

Ewa Obersztyn

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

Jacek Lenart

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

Jerzy Bal

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

P2860

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Cleft lip and palate: understanding genetic and environmental influences

Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

A combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.

Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases

Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development

Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes

IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population

P304

e161-7

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

P31

scholarly article

P356

10.1597/14-030

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

P407

English

P433

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

P478

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

P50

Jarosław Poznański

P577

2014-12-09T00:00:00Z

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

P698

25489771

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