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30. 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; 15(2):247-51. PubMed ID: 15647839 [TBL] [Abstract][Full Text] [Related]
31. BBBG syndrome or Opitz syndrome: new family. Verloes A; Le Merrer M; Briard ML Am J Med Genet; 1989 Nov; 34(3):313-6. PubMed ID: 2688419 [TBL] [Abstract][Full Text] [Related]
32. [Multiple hamartoma syndrome]. Pujol RM; Ravella A; Noguera X; de Moragas JM; Moreno A Med Cutan Ibero Lat Am; 1988; 16(4):322-7. PubMed ID: 3068443 [TBL] [Abstract][Full Text] [Related]
33. Cowden's disease with vocal fold involvement. To EW; Tsang WM; Pak MW; Cheng JH; Tse GM; van Hasselt CA Ear Nose Throat J; 2001 Oct; 80(10):754-6, 758. PubMed ID: 11605575 [TBL] [Abstract][Full Text] [Related]
34. [Pediatric pathology and oral diseases (the pediatric viewpoint)]. Macciotta A Mondo Ortod; 1978; 3(3):17-28. PubMed ID: 283306 [No Abstract] [Full Text] [Related]
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