A heritable cause of cleft lip and palate—Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis-Reference-Cited by-同舟云学术

A heritable cause of cleft lip and palate—Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis

Published:2009-06-18 Issue:2 Volume:169 Page:223-228
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Ferrero Giovanni Battista,Baldassarre Giuseppina,Panza Emanuele,Valenzise Mariella,Pippucci Tommaso,Mussa Alessandro,Pepe Ernesto,Seri Marco,Silengo Margherita Cirillo

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00431-009-1011-3.pdf

Reference20 articles.

1. Badovinac RL, Werler MM, Williams PL, Kelsey KT, Hayes C (2007) Folic acid-containing supplement consumption during pregnancy and risk for oral clefts: a meta-analysis. Birth Defects Res A Clin Mol Teratol 79:8–15

2. Cobourne MT (2004) The complex genetics of cleft lip and palate. Eur J Orthod 26:7–16

3. Fraser FC (1970) The genetics of cleft lip and cleft palate. Am J Hum Genet 22:336–352

4. Gorlin RJ, Cohen MMJ, Levin LS (2001) Syndromes of the head and neck. Oxford University Press, Oxford

5. Gundlach KK, Maus C (2006) Epidemiological studies on the frequency of clefts in Europe and world-wide. J Craniomaxillofac Surg 34(Suppl 2):1–2

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1. Early treatment of congenital syngnathia. A case report;J PEDIATR NEONATAL I;2018

2. Genomic expression in non syndromic cleft lip and palate patients: A review;Journal of Oral Biology and Craniofacial Research;2015-05

3. Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family;Genetics Research;2014

4. IRF6 mutations may not be a major cause of Van der Woude syndrome in India;European Journal of Pediatrics;2010-09-16

5. Epidemiology of Van der Woude syndrome from mutational analyses in affected patients from Pakistan;Clinical Genetics;2010-02-09