IRF6 mutations may not be a major cause of Van der Woude syndrome in India
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00431-010-1288-2.pdf
Reference3 articles.
1. Ali A, Singh SK, Raman R (2009) Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India. Cleft Palate-Craniofac J 46(5):541–544. doi: 10.1597/08-202.1
2. Ferrero GB, Baldassarre G, Panza E, Valenzise M, Pippucci T, Mussa A, Pepe E, Seri M, Silengo MC (2010) 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. Eur J Pediatr 169:223–228. doi: 10.1007/s00431-009-1011-3
3. Moghe GA, Kaur MS, Thomas AM, Raseswari T, Swapna M, Rao L (2010) The role of 9qh+ in phenotypic and genotypic heterogeneity in a Van der Woude syndrome pedigree. J Indian Soc Pedod Prev Dent 28(2):104–109. doi: 10.4103/0970-4388.66749
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Van der Woude Syndrome: IRF6 Mutations;The Indian Journal of Pediatrics;2019-08-29
2. Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family;Genetics Research;2014
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