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Syndromes Hay–Wells syndrome TP63 Rapp–Hodgkin syndrome Ectodermal dysplasia Ectrodactyly Universidade Estadual Paulista Júlio de Mesquita Filho Ectrodactyly–ectodermal dysplasia–cleft syndrome Limb–mammary syndrome Health Genodermatoses Rare diseases		Revista2Vol89ingles2_Layout 1 Add to Reading List Source URL: www.ncbi.nlm.nih.gov Download Document from Source Website File Size: 125,18 KB Share Document on Facebook

	7q21.3 Deletion involving enhancer sequences within the gene DYNC1I1 presents with intellectual disability and split hand-split foot malformation with decreased penetrance DocID: 1fWsO - View Document
	The human disease network ′ A-LProc Natl Acad Sci USA 104:Goh K-I, Cusick ME, Valle D, Childs B, Vidal M, Barabasi Urolithiasise Caffey DocID: 14S6x - View Document
	OCT4 as a target of miR-34a stimulates p63 but inhibits p53 to promote human cell transformation DocID: 102hg - View Document
	Novel p63 target genes involved in paracrine signaling and keratinocyte differentiation DocID: ZEu0 - View Document
	The human disease network ′ A-L[removed]Proc Natl Acad Sci USA 104:[removed]Goh K-I, Cusick ME, Valle D, Childs B, Vidal M, Barabasi Urolithiasise Caffey DocID: XDko - View Document