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Browsing by Author Ades, L.C.

Full Text	Issue Date	Title	Author(s)
	2011	Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder	Talkowski, M.E.; Mullegama, S.V.; Rosenfeld, J.A.; Bon, B.W. van; Shen, Y., et al
	2010	The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype.	Bon, B.W.M. van; Koolen, D.A.; Brueton, L.; McMullan, D.; Lichtenbelt, K.D., et al
	2007	EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation?	Maclean, K.; Holme, S.A.; Gilmour, E.; Taylor, M.; Scheffer, H., et al