DSpace at RU >

Browsing by Author Meitinger, T.

Full Text	Issue Date	Title	Author(s)
	2011	Large-scale gene-centric analysis identifies novel variants for coronary artery disease	Butterworth, A.S.; Braund, P.S.; Hardwick, R.J.; Saleheen, D.; Peden, J.F., et al
	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
	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