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Ophthalmic Genetics|June 23, 2010
Leber's hereditary optic neuropathy: clinical and molecular profile of a Brazilian sampleAndréa Trevas Maciel-Guerra, Luciene Maria Zanchetta, Marcela Scabello Amaral Fernandes, et al.Ophthalmic Genetics|June 23, 2010
Mutation screen of beta-crystallin genes in 274 patients with age-related macular degenerationGwen M Sturgill, Elisa Bala, Stacia S Yaniglos, et al.Ophthalmic Genetics|December 24, 2011
A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A geneAlina V Dumitrescu, Jeff M Milunsky, Susannah Q Longmuir, et al.Ophthalmic Genetics|January 11, 2012
Phenotype-genotype correlation in potential female carriers of X-linked developmental cataract (Nance-Horan syndrome)Arif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, et al.Ophthalmic Genetics|January 6, 2012
Identification of the p. R116H mutation in a Chinese family with novel variable cataract phenotype: evidence for a mutational hot spot in αA-crystallin geneBinbin Wang, Kai Jie Wang, Si Quan Zhu, et al.Ophthalmic Genetics|July 21, 2011
Retinoblastoma: lessons and challenges from developing countries. Ellsworth Lecture 2011Guillermo L ChantadaOphthalmic Genetics|August 17, 2011
Vitreous amyloidosis in two large mainland Chinese kindreds resulting from transthyretin variant Lys35Thr and Leu55ArgDa Long, Jun Zeng, Ling Qian Wu, et al.Ophthalmic Genetics|July 7, 2011
Proteasome modulator 9 gene is linked to diabetic and non-diabetic retinopathy in T2DClaudia GragnoliOphthalmic Genetics|April 23, 2011
Allelic and phenotypic heterogeneity in ABCA4 mutationsTomas R Burke, Stephen H TsangOphthalmic Genetics|March 17, 2011
Mutation screening of the GUCA1B gene in patients with autosomal dominant cone and cone rod dystrophyVeronique B D Kitiratschky, Christian Johannes Glöckner, Susanne KohlPageof 185