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Molecular Vision|July 1, 2005
Association between glaucoma and gene polymorphism of endothelin type A receptorKarin Ishikawa, Tomoyo Funayama, Yuichiro Ohtake, et al.Human Mutation|August 29, 2015
Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1Frauke Coppieters, Anne Laure Todeschini, Takuro Fujimaki, et al.Investigative Ophthalmology & Visual Science|November 24, 2004
Variants in optineurin gene and their association with tumor necrosis factor-alpha polymorphisms in Japanese patients with glaucomaTomoyo Funayama, Karin Ishikawa, Yuichiro Ohtake, et al.Human Mutation|October 26, 2022
Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencingAkiko Suga, Kazutoshi Yoshitake, Naoko Minematsu, et al.Pageof 3