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Investigative Ophthalmology & Visual Science|October 11, 2012
A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French PopulationWeihua Meng, Jacqueline Butterworth, Declan T Bradley, et al.
Journal of Vascular Surgery|October 3, 2008
C-reactive protein (CRP) elevation in patients with abdominal aortic aneurysm is independent of the most important CRP genetic polymorphismStephen A Badger, Chee V Soong, Mark E O'Donnell, et al.
Plos Medicine|December 29, 2007
Neovascular age-related macular degeneration risk based on CFH, LOC387715/HTRA1, and smokingAnne E Hughes, Nick Orr, Chris Patterson, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 18, 2004
Auditory perception and speech discrimination after cochlear implantation in patients with connexin 26 (GJB2) gene-related deafnessArasa Raj Sinnathuray, Joseph G Toner, Andrea Geddis, et al.
Investigative Ophthalmology & Visual Science|May 20, 2016
Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration RiskAnne E Hughes, Stephen Bridgett, Weihua Meng, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 18, 2004
Connexin 26 (GJB2) gene-related deafness and speech intelligibility after cochlear implantationArasa Raj Sinnathuray, Joseph G Toner, Joanne Clarke-Lyttle, et al.
Vascular Medicine (London, England)|February 6, 2010
Common polymorphisms of Fibulin-5 and the risk of abdominal aortic aneurysm developmentStephen A Badger, Chee V Soong, Mark E O'Donnell, et al.
Blood|October 24, 2002
Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductaseMelanie J Percy, Matthew J S Gillespie, Geraldine Savage, et al.
American Journal of Human Genetics|October 15, 2011
Mutation altering the miR-184 seed region causes familial keratoconus with cataractAnne E Hughes, Declan T Bradley, Malcolm Campbell, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Evidence for association of endothelial nitric oxide synthase gene in subjects with glaucoma and a history of migraineJoanne F J Logan, Usha Chakravarthy, Anne E Hughes, et al.
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