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Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Clinical & Experimental Ophthalmology|October 14, 2014
Pterygium and conjunctival ultraviolet autofluorescence in young Australian adults: the Raine studyCharlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
American Journal of Ophthalmology|July 30, 2014
Myopia in young adults is inversely related to an objective marker of ocular sun exposure: the Western Australian Raine cohort studyCharlotte M McKnight, Justin C Sherwin, Seyhan Yazar, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 15, 2010
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern GreeceGeorge Kitsos, Zacharias Petrou, Maria Grigoriadou, et al.
Scientific Reports|October 6, 2020
Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt diseaseJason Charng, Di Xiao, Maryam Mehdizadeh, et al.
BMJ Open|August 3, 2023
Study profile: the Genetics of Glaucoma StudyPuya Gharahkhani, Weixiong He, Santiago Diaz Torres, et al.
Investigative Ophthalmology & Visual Science|September 23, 2018
Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle GlaucomaLarry N Singh, Jonathan G Crowston, M Isabel G Lopez Sanchez, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|October 7, 2009
Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twinsDavid A Mackey, Jane R Mackinnon, Shayne A Brown, et al.
Investigative Ophthalmology & Visual Science|April 20, 2013
Copy number variation at chromosome 5q21.2 is associated with intraocular pressureAbhishek Nag, Cristina Venturini, Pirro G Hysi, et al.
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