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Ophthalmic Genetics|January 9, 2014
Sorting out co-occurrence of rare monogenic retinopathies: Stargardt disease co-existing with congenital stationary night blindnessNancy Huynh, Brett G Jeffrey, Amy Turriff, et al.Ophthalmic Genetics|February 18, 2015
Analysis of BAP1 Germline Gene Mutation in Young Uveal Melanoma PatientsColleen M Cebulla, Elaine M Binkley, Robert Pilarski, et al.Ophthalmic Genetics|June 30, 2020
Novel mutation in SLC4A7 gene causing autosomal recessive progressive rod-cone dystrophyJeeyun Ahn, John Chiang, Michael B GorinOphthalmic Genetics|June 30, 2020
No association between POU4F1, POU4F2, ISL1 polymorphisms and normal-tension glaucomaJee-Soo Lee, Jin Wook Jeoung, Sohee Oh, et al.Ophthalmic Genetics|July 7, 2020
Clinical and genetic study on two Chinese families with Wagner vitreoretinopathyHuajin Li, Hui Li, Lizhu Yang, et al.Ophthalmic Genetics|June 27, 2020
Oliver McFarlane syndrome and choroidal neovascularisation: a case reportAruni Kumari Makuloluwa, Rutika Dodeja, Michalis Georgiou, et al.Ophthalmic Genetics|August 8, 1998
Eye malformations associated with treatment with carbamazepine during pregnancyA G Sutcliffe, R B Jones, G WoodruffOphthalmic Genetics|July 20, 2012
Ten SNPs of PAX6, Lumican, and MYOC genes are not associated with high myopia in Han ChineseLili Dai, Ying Li, Chun Yu Du, et al.Ophthalmic Genetics|August 29, 2012
Ocular manifestations of the autoinflammatory syndromesAhmad Bakir Tarabishy, Amy G Hise, Elias I TraboulsiOphthalmic Genetics|April 26, 2022
The role of motor proteins in photoreceptor protein transport and visual functionRakesh Radhakrishnan, Venkateshwara R Dronamraju, Matthias Leung, et al.Pageof 185