1. Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.;Houdayer;Ann Genet,1999
2. A novel mutation, 1234del(c), of the IRF6 in a Thai family with van der Woude syndrome.;Shotelersuk;In J Mol Med,2003
3. Mutation in IRF6 causes van der Woude and popliteal pterygium syndrome.;Kondo;Nat Genet,2002
4. Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the van der Woude syndrome locus on 1q32.;Lees;J Med Genet,1999
5. Relationship between lower-lip fistulae and cleft lip and/or palate in van der Woude syndrome.;Onofre;Cleft Palate Craniofac,1997