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Browsing by Author Yzer, S.

Full Text	Issue Date	Title	Author(s)
	2007	Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays.	Hollander, A.I. den; Lopez, I.; Yzer, S.; Zonneveld, M.N.; Janssen, I.M., et al
	2007	Molecular and phenotypic analysis of a family with autosomal recessive cone-rod dystrophy and Stargardt disease.	Yzer, S.; Born, L.I. van den; Zonneveld, M.N.; Lopez, I.; Ayyagari, R., 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
	2006	Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.	Hollander, A.I. den; Koenekoop, R.K.; Yzer, S.; Lopez, I.; Arends, M.L., et al
	2006	CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis.	Yzer, S.; Fishman, G.A.; Racine, J.; Al-Zuhaibi, S.; Chakor, H., et al