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European Journal of Human Genetics : EJHG|April 19, 2021
A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataractJohanna L Jones, Mark A Corbett, Elise Yeaman, et al.
The British Journal of Ophthalmology|November 24, 2021
Conjunctival ultraviolet autofluorescence area decreases with age and sunglasses useGareth Lingham, Jason Kugelman, Jason Charng, et al.
Ophthalmology Science|October 17, 2022
Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus AutofluorescenceRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Investigative Ophthalmology & Visual Science|November 20, 2023
Changes in Refractive Error During Young Adulthood: The Effects of Longitudinal Screen Time, Ocular Sun Exposure, and Genetic PredispositionSamantha Sze-Yee Lee, Gareth Lingham, Carol A Wang, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
Ophthalmic Epidemiology|October 31, 2013
Birth order and myopiaJeremy A Guggenheim, George McMahon, Kate Northstone, et al.
Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
Investigative Ophthalmology & Visual Science|May 4, 2010
Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohortRavikanth Metlapally, Chang-Seok Ki, Yi-Ju Li, et al.
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