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535 related items for PubMed ID: 8588850
21. Identification of IRF6 gene variants in three families with Van der Woude syndrome. Tan EC, Lim EC, Yap SH, Lee ST, Cheng J, Por YC, Yeow V. Int J Mol Med; 2008 Jun; 21(6):747-51. PubMed ID: 18506368 [Abstract] [Full Text] [Related]
22. Orofacial clefting: update on the role of genetics. Ghassibe M, Bayet B, Revencu N, Desmyter L, Verellen-Dumoulin C, Gillerot Y, Deggouj N, Vanwijck R, Vikkula M, CL/P Study Group. B-ENT; 2006 Jun; 2 Suppl 4():20-4. PubMed ID: 17366841 [Abstract] [Full Text] [Related]
23. A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndrome. Shotelersuk V, Srichomthong C, Yoshiura K, Niikawa N. Int J Mol Med; 2003 Apr; 11(4):505-7. PubMed ID: 12632105 [Abstract] [Full Text] [Related]
26. Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome. Sander A, Schmelzle R, Murray J. Hum Mol Genet; 1994 Apr; 3(4):575-8. PubMed ID: 8069301 [Abstract] [Full Text] [Related]
28. A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome. Brosch S, Baur M, Blin N, Reinert S, Pfister M. Int J Mol Med; 2007 Jul; 20(1):85-9. PubMed ID: 17549393 [Abstract] [Full Text] [Related]
31. Van der Woude and Popliteal Pterygium Syndromes: Broad intrafamilial variability in a three generation family with mutation in IRF6. Busche A, Hehr U, Sieg P, Gillessen-Kaesbach G. Am J Med Genet A; 2016 Sep; 170(9):2404-7. PubMed ID: 27286731 [Abstract] [Full Text] [Related]
33. Van der Woude syndrome: a review of 11 cases seen at the Lagos University Teaching Hospital. James O, Adeyemo WL, Emeka CI, Ogunlewe MO, Ladeinde AL, Butali A. Afr J Paediatr Surg; 2014 Sep; 11(1):52-5. PubMed ID: 24647295 [Abstract] [Full Text] [Related]
34. Genetic epidemiology and control of genetic expression in van der Woude syndrome. Burdick AB. J Craniofac Genet Dev Biol Suppl; 1986 Sep; 2():99-105. PubMed ID: 3491128 [Abstract] [Full Text] [Related]
38. Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family. Manjegowda DS, Prasad M, Veerappa AM, Ramachandra NB. Genet Res (Camb); 2014 Oct 10; 96():e12. PubMed ID: 25579819 [Abstract] [Full Text] [Related]
40. A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude syndrome. Miñones-Suárez L, Mas-Vidal A, Fernandez-Toral J, Llano-Rivas I, González-García M. Pediatr Dermatol; 2012 Oct 10; 29(6):768-70. PubMed ID: 21995291 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]