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Browsing by Author Duijf, P.H.

Full Text	Issue Date	Title	Author(s)
	2008	A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromes.	Rinne, T.K.; Clements, S.E.; Lamme, E.; Duijf, P.H.; Bolat, E., et al
	2006	Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.	Rinne, T.K.; Spadoni, E.; Kjaer, K.W.; Danesino, C.; Larizza, D., et al
	2005	Molecular Genetics of EEC Syndrome and Related Disorders.	Duijf, P.H.
	2005	Ectodermal dysplasia: skinny models on the catwalk.	Duijf, P.H.; Bokhoven, J.H.L.M. van
	2004	Mutations in the human TBX4 gene cause small patella syndrome.	Bongers, M.H.F.; Duijf, P.H.; Beersum, S.E.C. van; Schoots, J.; Kampen, A. van, et al