Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population (Q34446991)

2 August 2017

title

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population (English)

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cleft lip with or without cleft palate

2 August 2017

main subject

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7

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Christine Verellen-Dumoulin

2 August 2017

4

object named as

Christine Verellen-Dumoulin

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2 August 2017

Michella Ghassibé

1

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2 August 2017

Benedicte Bayet

2

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2 August 2017

Nicole Revencu

3

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2 August 2017

Yves Gillerot

5

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2 August 2017

Romain Vanwijck

6

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2 August 2017

publication date

1 November 2005

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European Journal of Human Genetics

2 August 2017

published in

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2 August 2017

volume

13

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2 August 2017

issue

11

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2 August 2017

page(s)

1239-1242

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Cleft palate: players, pathways, and pursuits

2 August 2017

cites work

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

Identification of SATB2 as the cleft palate gene on 2q32-q33.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

Gene/environment causes of cleft lip and/or palate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

The many faces and factors of orofacial clefts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

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/10.1038%2FSJ.EJHG.5201486

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

The family based association test method: strategies for studying general genotype--phenotype associations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

GOLD--graphical overview of linkage disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

inferred from DOI database lookup

7 January 2021

based on heuristic

The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201486

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201486

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2 August 2017

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