Condition: RAPP-HODGKIN SYNDROME


rs121908840 in TP63 gene and RAPP-HODGKIN SYNDROME PMID 12939657 2003 The Rapp-Hodgkin syndrome results from mutations of the TP63 gene.

PMID 15200513 2004 Molecular evidence that AEC syndrome and Rapp-Hodgkin syndrome are variable expression of a single genetic disorder.

PMID 12766194 2003 Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia.