Ectodermal Dysplasia: Rapp-Hodgkin Syndrome and Hay-Wells Syndrome
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Elsevier
Reference77 articles.
1. Differential PERP regulation by TP63 mutants provides insight into AEC pathogenesis;Beaudry;American Journal of Medical Genetics Part A,2009
2. Molecular evidence that AEC syndrome and Rapp-Hodgkin syndrome are variable expression of a single genetic disorder;Bertola;Clinical Genetics,2004
3. Splitting p63;van Bokhoven;American Journal of Human Genetics,2002
4. p63 gene mutations in EEC syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation;van Bokhoven;American Journal of Human Genetics,2001
5. The Rapp-Hodgkin syndrome results from mutations of the TP63 gene;Bougeard;European Journal of Human Genetics: EJHG,2003
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