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5. The p63 gene in EEC and other syndromes. Brunner HG; Hamel BC; Van Bokhoven H J Med Genet; 2002 Jun; 39(6):377-81. PubMed ID: 12070241 [TBL] [Abstract][Full Text] [Related]
6. p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly. Berdón-Zapata V; Granillo-Alvarez M; Valdés-Flores M; García-Ortiz JE; Kofman-Alfaro S; Zenteno JC J Orthop Res; 2004 Jan; 22(1):1-5. PubMed ID: 14656652 [TBL] [Abstract][Full Text] [Related]
7. P63 gene mutations and human developmental syndromes. Brunner HG; Hamel BC; Bokhoven Hv Hv Am J Med Genet; 2002 Oct; 112(3):284-90. PubMed ID: 12357472 [TBL] [Abstract][Full Text] [Related]
8. Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation. Clements SE; Techanukul T; Coman D; Mellerio JE; McGrath JA Br J Dermatol; 2010 Jan; 162(1):201-7. PubMed ID: 19903181 [TBL] [Abstract][Full Text] [Related]
9. Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts. Barrow LL; van Bokhoven H; Daack-Hirsch S; Andersen T; van Beersum SE; Gorlin R; Murray JC J Med Genet; 2002 Aug; 39(8):559-66. PubMed ID: 12161593 [TBL] [Abstract][Full Text] [Related]
10. p63-associated disorders. Rinne T; Brunner HG; van Bokhoven H Cell Cycle; 2007 Feb; 6(3):262-8. PubMed ID: 17224651 [TBL] [Abstract][Full Text] [Related]
11. R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy. Valenzise M; Arrigo T; De Luca F; Privitera A; Frigiola A; Carando A; Garelli E; Silengo M Eur J Med Genet; 2008; 51(5):497-500. PubMed ID: 18603493 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Light in the confusion of ectodermal dysplasia syndrome. Mutations in p63 gene induce different phenotype expressions]. Krutmann J; Funk JO; Korge B Hautarzt; 2001 Sep; 52(9):851-2. PubMed ID: 11693108 [No Abstract] [Full Text] [Related]
14. Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia. Kantaputra PN; Hamada T; Kumchai T; McGrath JA J Dent Res; 2003 Jun; 82(6):433-7. PubMed ID: 12766194 [TBL] [Abstract][Full Text] [Related]
15. The EEC syndrome and SHFM: report of two cases and mutation analysis of p63 gene. Ergin H; Semerci CN; Karakuş YT; Scheffer H; Ergin S; Koltuksuz U; Meijer R; Satiroğlu-Tufan NL Turk J Pediatr; 2010; 52(5):529-33. PubMed ID: 21434540 [TBL] [Abstract][Full Text] [Related]
16. Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype. Paranaíba LM; Martelli-Júnior H; de Miranda RT; Bufalino A; Abdo Filho RC; Coletta RD Cleft Palate Craniofac J; 2010 Sep; 47(5):544-7. PubMed ID: 20180707 [TBL] [Abstract][Full Text] [Related]
17. A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting. Sorasio L; Biamino E; Garelli E; Ferrero GB; Silengo MC Clin Exp Dermatol; 2009 Dec; 34(8):e726-8. PubMed ID: 19663851 [TBL] [Abstract][Full Text] [Related]
18. Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63. McGrath JA; Duijf PH; Doetsch V; Irvine AD; de Waal R; Vanmolkot KR; Wessagowit V; Kelly A; Atherton DJ; Griffiths WA; Orlow SJ; van Haeringen A; Ausems MG; Yang A; McKeon F; Bamshad MA; Brunner HG; Hamel BC; van Bokhoven H Hum Mol Genet; 2001 Feb; 10(3):221-9. PubMed ID: 11159940 [TBL] [Abstract][Full Text] [Related]
19. A de novo heterozygous point mutation in the p63 gene causing the syndrome of ectrodactyly, ectodermal dysplasia and facial clefting. Pozo G; Canún S; Kofman-Alfaro S; Zenteno JC Br J Dermatol; 2004 Oct; 151(4):930-2. PubMed ID: 15491445 [No Abstract] [Full Text] [Related]
20. An unusual combination of EEC syndrome and hypomelanosis Ito due to a p63 mutation. Lehmann K; Mundlos S; Meinecke P Eur J Pediatr; 2005 Aug; 164(8):530-1. PubMed ID: 15889277 [No Abstract] [Full Text] [Related] [Next] [New Search]