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Browsing by Author Weston, M.D.

Full Text	Issue Date	Title	Author(s)
	2007	Development of a genotyping microarray for Usher syndrome.	Cremers, F.P.M.; Kimberling, W.J.; Kulm, M.; Brouwer, A.P.M. de; Wijk, E. van, et al
	2004	USH2A mutation analysis in 70 Dutch families with Usher syndrome type II.	Pennings, R.J.E.; Brinke, H. te; Weston, M.D.; Claassen, A.M.W.; Orten, D.J., et al
	2004	Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.	Weston, M.D.; Luijendijk, M.W.J.; Humphrey, K.D.; Moller, C.G.; Kimberling, W.J.
	1995	Gene mapping of the Usher syndrome type IIa : Localization of the gene to a 2.1-cM segment on chromosome 1q41.	Kimberling, W.J.; Weston, M.D.; Moller, C.G.; Aarem, A. van; Cremers, C.W.R.J., et al
	1995	Defective myosin VIIA gene responsible for Usher syndrome type 1B	Well, D.; Blanchard, S.; Kaplan, J.; Guilford, P.; Gibson, F., et al