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Archives of Ophthalmology (Chicago, Ill. : 1960)|August 13, 2003
Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutationDavid A Mackey, Danielle L Healey, John H Fingert, et al.
Genetic Epidemiology|October 27, 2015
Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization StudyGabriel Cuellar-Partida, Yi Lu, Pik Fang Kho, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 10, 2003
Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentationsJamie E Craig, J Benedict Clark, Janet L McLeod, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathyCarmel Toomes, Helen M Bottomley, Sheila Scott, et al.
Hypertension (Dallas, Tex. : 1979)|August 19, 2009
Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye StudyCong Sun, Gu Zhu, Tien Y Wong, et al.
European Journal of Human Genetics : EJHG|October 3, 2008
Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic diseaseLiesel M FitzGerald, Briony Patterson, Russell Thomson, et al.
Ophthalmology|January 21, 2016
A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal ErosionsVerity F Oliver, Katherine A van Bysterveldt, Murray Cadzow, et al.
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