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Browsing by Author Wilson, M.

Full Text	Issue Date	Title	Author(s)
	2009	Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.	Kleefstra, T.; Zelst-Stams, W.A. van; Nillesen, W.M., et al
	2010	Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus.	Kouwenhoven, E.N.; Heeringen, S.J. van; Tena, J.J., et al
	2008	Visually assessed breast density, breast cancer risk and the importance of the craniocaudal view.	Duffy, S.W.; Nagtegaal, I.D.; Astley, S.M., et al