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Ophthalmic Genetics|April 26, 2000
Identification of a novel mutation in the paired domain of PAX3 in an Iranian family with waardenburg syndrome type IV N Sotirova, T M Rezaie, M M Khoshsorour, et al.Ophthalmic Genetics|July 13, 2001
Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotypeQ Zhang, S Li, X Guo, et al.Ophthalmic Genetics|September 18, 2001
Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosaK Zhao, S Xiong, L Wang, et al.Ophthalmic Genetics|September 18, 2001
Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosaK Zhao, L Wang, L Wang, et al.Ophthalmic Genetics|October 3, 2019
A new novel nonsense mutation in AIPL1 in a LCA4 familyLing Wan, Li Xiang, Haixin Wang, et al.Ophthalmic Genetics|September 13, 2019
Sjögren-Larsson syndrome: a complex metabolic disease with a distinctive ocular phenotypeSamiksha Fouzdar-Jain, Donny W Suh, William B RizzoOphthalmic Genetics|August 27, 2020
Association study of toll-like receptors 4 polymorphisms and the risk of age-related macular degeneration: a meta-analysisJian-Ying Zhou, Yi-Qian Huang, Xiao-Yan Zhang, et al.Ophthalmic Genetics|March 10, 2011
An atypical form of Bietti crystalline dystrophySettimio Rossi, Francesco Testa, Anren Li, et al.Ophthalmic Genetics|April 1, 2011
The optic nerve head in congenital fibrosis of the extraocular musclesArif O Khan, Jameela Shinwari, Aisha Omar, et al.Ophthalmic Genetics|May 20, 2011
Horizontal gaze palsy and progressive scoliosis due to a deleterious mutation in ROBO3Khaled K Abu-Amero, Seema Kapoor, Ali Hellani, et al.Pageof 185