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Ophthalmic Genetics|December 29, 2007
Severe form of familial exudative vitreoretinopathy caused by homozygous R417Q mutation in frizzled-4 geneHiroyuki Kondo, Minghui Qin, Tomoko Tahira, et al.Ophthalmic Genetics|December 29, 2007
Genetic screening of leber congenital amaurosis in a large consanguineous Iranian familyTayebeh Rezaie, Mohammad-Hassan Karimi-Nejad, Mohammad-Reza Meshkat, et al.Ophthalmic Genetics|March 22, 2017
Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closureJin Wook Jeoung, Jung Hwa Ko, Yu Jeong Kim, et al.Ophthalmic Genetics|March 15, 2021
Clinical diagnosis of presumed SOX2 gonadosomatic mosaicismMalena Daich Varela, Robert B Hufnagel, Bin Guan, et al.Ophthalmic Genetics|November 8, 2021
Pathogenic variants in the CYP21A2 gene cause isolated autosomal dominant congenital posterior polar cataractsVanita Berry, Nikolas Pontikos, Alex Ionides, et al.Ophthalmic Genetics|November 10, 2012
Role of rs1533428 and rs12994401 in patients with Primary Open Angle Glaucoma in an European populationAlexander Bachernegg, Yosuf El-Shabrawi, Martin Weger, et al.Ophthalmic Genetics|November 14, 2012
Absence of an association between lumican promoter variants and high myopia in the Korean populationShin Hae Park, Jeewon Mok, Choun-Ki JooOphthalmic Genetics|May 16, 2014
Next-generation sequencing revealed a novel mutation in the gene encoding the beta subunit of rod phosphodiesteraseSherry Shen, Tharikarn Sujirakul, Stephen H TsangOphthalmic Genetics|January 15, 2014
Ocular Features in 16 Brazilian Patients with Williams-Beuren SyndromeMelissa Machado Viana, Maria Frasson, Henrique Galvão, et al.Ophthalmic Genetics|January 17, 2014
Early-Onset X-Linked Retinitis Pigmentosa in a Heterozygous Female Harboring an Intronic Donor Splice Site Mutation in the Retinitis Pigmentosa GTPase Regulator GeneAmde Selassie Shifera, Christine Nichols KayPageof 185