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Browsing by Author Hurst, J.A.

Full Text	Issue Date	Title	Author(s)
	2008	Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.	Koolen, D.A.; Sharp, A.J.; Hurst, J.A.; Firth, H.V.; Knight, S.J., et al
	2005	Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation.	Koolen, D.A.; Reardon, W.; Rosser, E.M.; Lacombe, D.; Hurst, J.A., et al
	2004	Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.	Vissers, L.E.L.M.; Ravenswaaij-Arts, C.M.A. van; Admiraal, R.J.C.; Hurst, J.A.; Vries, L.B.A. de, et al