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2. Van der Woude syndrome: dentofacial features and implications for clinical practice. Lam AK, David DJ, Townsend GC, Anderson PJ. Aust Dent J; 2010 Mar; 55(1):51-8. PubMed ID: 20415912 [Abstract] [Full Text] [Related]
3. Genetic epidemiology and control of genetic expression in van der Woude syndrome. Burdick AB. J Craniofac Genet Dev Biol Suppl; 1986 Mar; 2():99-105. PubMed ID: 3491128 [Abstract] [Full Text] [Related]
4. [Van-der-Woude Syndrome]. Del Frari B, Amort M, Janecke AR, Schutte BC, Piza-Katzer H. Klin Padiatr; 2008 Mar; 220(1):26-8. PubMed ID: 18095255 [Abstract] [Full Text] [Related]
7. [Dominantly inherited lower lip fistulas and facial clefts (Van der Woude syndrome). A study of 52 cases]. Kläusler M, Schinzel A, Gnoinski W, Hotz M, Perko M. Schweiz Med Wochenschr; 1987 Jan 24; 117(4):127-34. PubMed ID: 3823824 [Abstract] [Full Text] [Related]
9. Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation. Beiraghi S, Miller-Chisholm A, Kimberling WJ, Sun CE, Wang YF, Russell LJ, Khoshnevisan M, Storm AL, Long RE, Witt PD, Mazaheri M, Diehl SR. J Craniofac Genet Dev Biol; 1999 Jan 24; 19(3):128-34. PubMed ID: 10589394 [Abstract] [Full Text] [Related]
11. 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 24; 11(4):505-7. PubMed ID: 12632105 [Abstract] [Full Text] [Related]
12. Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family. Item CB, Turhani D, Thurnher D, Yerit K, Sinko K, Wittwer G, Adeyemo WL, Frei K, Erginel-Unaltuna N, Watzinger F, Ewers R. Int J Mol Med; 2005 Feb 24; 15(2):247-51. PubMed ID: 15647839 [Abstract] [Full Text] [Related]
14. Lower lip pits in a patient with van der Woude syndrome. Baghestani S, Sadeghi N, Yavarian M, Alghasi H. J Craniofac Surg; 2010 Sep 24; 21(5):1380-1. PubMed ID: 20818247 [Abstract] [Full Text] [Related]
19. 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 24; 21(6):747-51. PubMed ID: 18506368 [Abstract] [Full Text] [Related]
20. The van der Woude syndrome in a large kindred: variability, penetrance, genetic risks. Janku P, Robinow M, Kelly T, Bralley R, Baynes A, Edgerton MT. Am J Med Genet; 1980 Jun 24; 5(2):117-23. PubMed ID: 7395906 [Abstract] [Full Text] [Related] Page: [Next] [New Search]