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Molecular Vision|March 23, 2026
Molecular insights into foveal hypoplasia: development, genetics, mechanisms, and modelsKevin Gregory-Evans, Cheryl Y Gregory-EvansBiochemical and Biophysical Research Communications|January 8, 1999
Sequence and tissue expression of a novel human carbonic anhydrase-related protein, CARP-2, mapping to chromosome 19q13.3J Bellingham, K Gregory-Evans, C Y Gregory-EvansHuman Genetics|January 4, 2019
Prospects and modalities for the treatment of genetic ocular anomaliesCheryl Y Gregory-Evans, Xia Wang, Kevin Gregory-EvansAnnals of Human Genetics|November 6, 1998
Mapping of human interferon regulatory factor 3 (IRF3) to chromosome 19q13.3-13.4 by an intragenic polymorphic markerJ Bellingham, K Gregory-Evans, C Y Gregory-EvansHandbook of Clinical Neurology|April 9, 2021
A review of diseases of the retina for neurologistsKevin Gregory-EvansMolecular Vision|July 3, 2025
Mutation of beta-tubulin 4B gene (<i>TUBB4B)</i> causes autosomal dominant retinitis pigmentosa with sensorineural hearing loss in a multigenerational familyCheryl Y Gregory-Evans, Aaron W Joe, Kevin Gregory-EvansProgress in Retinal and Eye Research|November 7, 2012
Gene networks: dissecting pathways in retinal development and diseaseCheryl Y Gregory-Evans, Valerie A Wallace, Kevin Gregory-EvansHuman Genetics|May 11, 2019
An update on the genetics of ocular colobomaAisha S ALSomiry, Cheryl Y Gregory-Evans, Kevin Gregory-EvansMolecular Vision|June 17, 2011
Gene-specific differential response to anti-apoptotic therapies in zebrafish models of ocular colobomaCheryl Y Gregory-Evans, Mariya Moosajee, Xianghong Shan, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|January 15, 2026
Genotypic and phenotypic landscape of novel RPGR variants in patients from Western CanadaCheryl Y Gregory-Evans, Maheshver Shunmugam, Boaz Li, et al.Pageof 13