kw.\*:("Syndrome de Rapp-Hodgkin")
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Functional Characterization of a Novel TP63 Mutation in a Family With Overlapping Features of Rapp-Hodgkin/AEC/ADULT SyndromesSERRA, Valeria; CASTORI, Marco; PARADISI, Mauro et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 3104-3109, issn 1552-4825, 6 p.Article
A new mutation in TP63 is associated with age-related pathologyHOLDER-ESPINASSE, Muriel; MARTIN-COIGNARD, Dominique; ESCANDE, Fabienne et al.European journal of human genetics. 2007, Vol 15, Num 11, pp 1115-1120, issn 1018-4813, 6 p.Article
Skin symptoms in four ectodermal dysplasia syndromes including two case reports of Rapp-Hodgkin-SyndromeKNAUDT, Bjorn; VOLZ, Thomas; KRUG, Markus et al.EJD. European journal of dermatology. 2012, Vol 22, Num 5, pp 605-613, issn 1167-1122, 9 p.Article
Rapp―Hodgkin and Hay―Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorderCLEMENTS, S. E; TECHANUKUL, T; HOLDEN, S. T et al.British journal of dermatology (1951). 2010, Vol 163, Num 3, pp 624-629, issn 0007-0963, 6 p.Article
Mutati in SAM Domain of TP63 is Associated With Nonsyndromic Cleft Lip and Palate and Cleft PalateKANTAPUTRA, Piranit N; MALAIVIJITNOND, Sutti; VIEIRA, Alexandre R et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 6, pp 1432-1436, issn 1552-4825, 5 p.Article