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Browsing by Author Leroy, B.P.

Full Text	Issue Date	Title	Author(s)
	2011	Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response	Wissinger, B.; Schaich, S.; Baumann, B.; Bonin, M.; Jagle, H., et al
	2010	Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients.	Hoornaert, K.P.; Vereecke, I.; Dewinter, C.; Rosenberg, T.; Beemer, F.A., et al
	2009	Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.	Thiadens, A.A.H.J.; Hollander, A.I. den; Roosing, S.; Nabuurs, S.B.; Zekveld-Vroon, R.C., et al
	2009	The spectrum of ocular phenotypes caused by mutations in the BEST1 gene.	Boon, C.J.F.; Klevering, B.J.; Leroy, B.P.; Hoyng, C.B.; Keunen, J.E.E., et al
	2009	Genotyping microarray for CSNB-associated genes.	Zeitz, C.; Labs, S.; Lorenz, B.; Forster, U.; Uksti, J., et al
	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
	2006	Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosis.	Yzer, S.; Leroy, B.P.; Baere, E. de; Ravel, T.J. de; Zonneveld-Vrieling, M.N., et al