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Investigative Ophthalmology & Visual Science|June 7, 2011
Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genesJianjun Chen, Nizar Smaoui, Monia Ben Hamed Hammer, et al.
Nature|January 1, 2004
Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivationKoji M Nishiguchi, Michael A Sandberg, Aart C Kooijman, et al.
The Journal of Biological Chemistry|September 7, 2002
Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation functionXuejiao Wang, Siqun Xu, Carlo Rivolta, et al.
Investigative Ophthalmology & Visual Science|December 4, 2014
Targeted exon sequencing in Usher syndrome type IKinga M Bujakowska, Mark Consugar, Emily Place, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 15, 2004
Further evaluation of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment: subgroup analysesEliot L Berson, Bernard Rosner, Michael A Sandberg, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 15, 2004
Clinical trial of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatmentEliot L Berson, Bernard Rosner, Michael A Sandberg, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 14, 2010
Clinical trial of lutein in patients with retinitis pigmentosa receiving vitamin AEliot L Berson, Bernard Rosner, Michael A Sandberg, et al.
Investigative Ophthalmology & Visual Science|May 31, 2002
Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseasesDror Sharon, Hiroyuki Yamamoto, Terri L McGee, et al.
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