Showing results (391-400 of 458) with videos related to

Sort By:
Pageof 46
American Journal of Human Genetics|December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.
Investigative Ophthalmology & Visual Science|April 28, 2021
IMI 2021 Yearly DigestMonica Jong, Jost B Jonas, James S Wolffsohn, et al.
Nature Genetics|June 29, 2023
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk lociXikun Han, Puya Gharahkhani, Andrew R Hamel, et al.
Human Molecular Genetics|June 7, 2015
WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thicknessGabriel Cuellar-Partida, Henriët Springelkamp, Sionne E M Lucas, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)Koki Yamada, Wai-Man Chan, Caroline Andrews, et al.
American Journal of Ophthalmology|May 24, 2019
Genetic Correlations Between Diabetes and Glaucoma: An Analysis of Continuous and Dichotomous PhenotypesVincent Laville, Jae H Kang, Clara C Cousins, et al.
Nature Communications|July 26, 2022
Transcriptomic and proteomic retinal pigment epithelium signatures of age-related macular degenerationAnne Senabouth, Maciej Daniszewski, Grace E Lidgerwood, et al.
Pageof 46