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Browsing by Author Baere, E. de

Full Text	Issue Date	Title	Author(s)
	2012	A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia.	Kohl, S.; Coppieters, F.; Meire, F.; Schaich, S.; Roosing, S., et al
	2011	Corrigendum: Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.	Radstake, T.R.D.J.; Gorlova, O.; Rueda, B.; Martin, J.E.; Alizadeh, B.Z., et al
	2011	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy	Gorlova, O.; Martin, J.E.; Rueda, B.; Koeleman, B.P.; Ying, J., et al
	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	Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.	Radstake, T.R.D.J.; Gorlova, O.; Rueda, B.; Martin, J.E.; Alizadeh, B.Z., et al
	2009	Genotyping microarray for CSNB-associated genes.	Zeitz, C.; Labs, S.; Lorenz, B.; Forster, U.; Uksti, J., 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
	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