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2. De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome. Shotelersuk V; Janklat S; Siriwan P; Tongkobpetch S Clin Exp Dermatol; 2005 May; 30(3):282-5. PubMed ID: 15807690 [TBL] [Abstract][Full Text] [Related]
3. Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child. Moerman P; Fryns JP Am J Med Genet; 1996 Jun; 63(3):479-81. PubMed ID: 8737656 [TBL] [Abstract][Full Text] [Related]
5. Molecular evidence that AEC syndrome and Rapp-Hodgkin syndrome are variable expression of a single genetic disorder. Bertola DR; Kim CA; Albano LM; Scheffer H; Meijer R; van Bokhoven H Clin Genet; 2004 Jul; 66(1):79-80. PubMed ID: 15200513 [No Abstract] [Full Text] [Related]
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7. AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndrome. Sorasio L; Ferrero GB; Garelli E; Brunello G; Martano C; Carando A; Belligni E; Dianzani I; Cirillo Silengo M Eur J Med Genet; 2006; 49(6):520-2. PubMed ID: 16824815 [No Abstract] [Full Text] [Related]
8. Scalp dermatitis, ectodermal dysplasia and cleft lip and palate: rapp-hodgkin or AEC syndrome. Rowan DM Australas J Dermatol; 1996 May; 37(2):102-3. PubMed ID: 8687323 [TBL] [Abstract][Full Text] [Related]
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17. Hay-Wells syndrome in a child with mutation in the TP73L gene. Garcia Bartels N; Neumann LM; Mleczko A; Rubach K; Peters H; Rossi R; Sterry W; Blume-Peytavi U J Dtsch Dermatol Ges; 2007 Oct; 5(10):919-23. PubMed ID: 17910675 [TBL] [Abstract][Full Text] [Related]
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