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Browsing by Author Schooneveld, M.J. van

Full Text	Issue Date	Title	Author(s)
	2011	High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative of autosomal recessive RP in the Dutch population	Collin, R.W.J.; Born, L.I. van den; Klevering, B.J.; Castro-Miro, M. de; Littink, K.W., et al
	2010	Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.	Booij, J.C.; Boon, C.J.F.; Schooneveld, M.J. van; Brink, J.B. ten; Bakker, A., et al
	2010	Homozygosity mapping in patients with cone-rod dystrophy: novel mutations and clinical characterizations.	Littink, K.W.; Koenekoop, R.K.; Born, L.I. van den; Collin, R.W.J.; Moruz, L.M., et al
	2010	Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophy	Thiadens, A.A.H.J.; Roosing, S.; Collin, R.W.J.; Moll-Ramirez, N. van; Lith-Verhoeven, J.J. van, et al
	2010	Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography.	Thiadens, A.A.H.J.; Somervuo, V.; Born, L.I. van den; Roosing, S.; Schooneveld, M.J. van, et al
	2009	Clinical and molecular genetic analysis of best vitelliform macular dystrophy.	Boon, C.J.F.; Theelen, T.; Hoefsloot, L.H.; Schooneveld, M.J. van; Keunen, J.E.E., 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	Genetic etiology and clinical consequences of complete and incomplete achromatopsia	Thiadens, A.A.H.J.; Slingerland, N.W.; Roosing, S.; Schooneveld, M.J. van; Lith-Verhoeven, J.J. van, et al
	2007	Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus.	Boon, C.J.F.; Schooneveld, M.J. van; Hollander, A.I. den; Lith-Verhoeven, J.J. van; Zonneveld-Vrieling, M.N., et al