Literature DB >> 20845047

IRF6 mutations may not be a major cause of Van der Woude syndrome in India.

Gayatri A Moghe, Simratvir Mauli.   

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Year:  2010        PMID： 20845047     DOI： 10.1007/s00431-010-1288-2

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  3 in total

1.  Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India.

Authors:  Akhtar Ali; Subodh Kumar Singh; Rajiva Raman
Journal:  Cleft Palate Craniofac J       Date:  2009-03-02

2.  The role of 9qh+ in phenotypic and genotypic heterogeneity in a Van der Woude syndrome pedigree.

Authors:  G A Moghe; M S Kaur; A M Thomas; T Raseswari; M Swapna; L Rao
Journal:  J Indian Soc Pedod Prev Dent       Date:  2010 Apr-Jun

3.  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.

Authors:  Giovanni Battista Ferrero; Giuseppina Baldassarre; Emanuele Panza; Mariella Valenzise; Tommaso Pippucci; Alessandro Mussa; Ernesto Pepe; Marco Seri; Margherita Cirillo Silengo
Journal:  Eur J Pediatr       Date:  2009-06-18       Impact factor: 3.183
  3 in total
  1 in total

1.  Van der Woude Syndrome: IRF6 Mutations.

Authors:  Ansa P Sunny; Gautham Arunachal; Sumita Danda
Journal:  Indian J Pediatr       Date:  2019-08-29       Impact factor: 1.967
  1 in total

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