(Q52006307)

19 April 2018

title

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

1 reference

19 April 2018

author name string

X Du

1

1 reference

19 April 2018

W Tang

2

1 reference

19 April 2018

W Tian

3

1 reference

19 April 2018

S Li

4

1 reference

19 April 2018

X Li

5

1 reference

19 April 2018

L Liu

6

1 reference

19 April 2018

X Zheng

7

1 reference

19 April 2018

X Chen

8

1 reference

19 April 2018

Y Lin

9

1 reference

19 April 2018

Y Tang

10

1 reference

19 April 2018

language of work or name

English

0 references

publication date

1 October 2006

1 reference

19 April 2018

Journal of Dental Research

published in

1 reference

19 April 2018

volume

85

1 reference

19 April 2018

issue

10

1 reference

19 April 2018

page(s)

937-940

1 reference

19 April 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

Novel mutation of the initiation codon of PAX9 causes oligodontia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

Interferon regulatory factors: the next generation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910608501013

10.1177/154405910608501013

21 January 2018

Identifiers

DOI

1 reference

19 April 2018

PubMed ID

16998136

1 reference

19 April 2018