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3. 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]
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]
5. The penetrance and variable expression of the Van der Woude syndrome: implications for genetic counseling. Shprintzen RJ, Goldberg RB, Sidoti EJ. Cleft Palate J; 1980 Jan; 17(1):52-7. PubMed ID: 6928118 [Abstract] [Full Text] [Related]
6. 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 Jan; 5(2):117-23. PubMed ID: 7395906 [Abstract] [Full Text] [Related]
7. Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34. Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J. Eur J Hum Genet; 2001 Oct; 9(10):747-52. PubMed ID: 11781685 [Abstract] [Full Text] [Related]
9. van der Woude syndrome in two families in China. Burdick AB, Ma LA, Dai ZH, Gao NN. J Craniofac Genet Dev Biol; 1987 Oct; 7(4):413-8. PubMed ID: 3429616 [Abstract] [Full Text] [Related]
10. 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 Oct; 2 Suppl 4():20-4. PubMed ID: 17366841 [Abstract] [Full Text] [Related]
12. Report of two cases with Van der Woude syndrome: a child and her mother. Koçer U, Aksoy HM, Tiftikcioğlu YO, Cöloğlu H, Karaaslan O. Genet Couns; 2001 Oct; 12(4):341-6. PubMed ID: 11837602 [Abstract] [Full Text] [Related]
13. [Genetic analysis of two families with van der Woude's syndrome (lip pits, cleft palate, and cleft lip syndrome)]. Burdick AB, Ma LA, Gao N, Dai ZH. Yi Chuan Xue Bao; 1988 Oct; 15(5):396-400. PubMed ID: 3273683 [No Abstract] [Full Text] [Related]
14. Van der Woude syndrome--recognition of lesser expressions: case report. Menko FH, Koedijk PH, Baart JA, Kwee ML. Cleft Palate J; 1988 Jul; 25(3):318-21. PubMed ID: 3168277 [Abstract] [Full Text] [Related]
16. A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndrome. Gatta V, Scarciolla O, Cupaioli M, Palka C, Chiesa PL, Stuppia L. Mutat Res; 2004 Mar 22; 547(1-2):49-53. PubMed ID: 15013698 [Abstract] [Full Text] [Related]
17. The role of 9qh+ in phenotypic and genotypic heterogeneity in a Van der Woude syndrome pedigree. Moghe GA, Kaur MS, Thomas AM, Raseswari T, Swapna M, Rao L. J Indian Soc Pedod Prev Dent; 2010 Mar 22; 28(2):104-9. PubMed ID: 20660977 [Abstract] [Full Text] [Related]
18. [Lower lip and cleft lip with "pits" (Van der Woude syndrome). Study in a family (author's transl)]. Guízar-Vázquez J, Armendares S. Rev Invest Clin; 1975 Mar 22; 27(4):295-9. PubMed ID: 1215696 [No Abstract] [Full Text] [Related]
19. 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 22; 15(2):247-51. PubMed ID: 15647839 [Abstract] [Full Text] [Related]
20. 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 22; 11(4):505-7. PubMed ID: 12632105 [Abstract] [Full Text] [Related] Page: [Next] [New Search]