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Neuroscience Letters|February 23, 2013
Novel GUCA1A mutation identified in a Chinese family with cone-rod dystrophyLi Huang, Shiqiang Li, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|August 30, 2024
The Systemic Genotype-Phenotype Characterization of PAX6-Related Eye Disease in 164 Chinese FamiliesYi Jiang, Zhen Yi, Yuxi Zheng, et al.
Investigative Ophthalmology & Visual Science|January 10, 2016
Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet GenesWenmin Sun, Li Huang, Yan Xu, et al.
Molecular Vision|March 9, 2010
Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopiaQin Wang, Panfeng Wang, Shiqiang Li, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|November 20, 2015
Identification of MFRP Mutations in Chinese Families with High HyperopiaYan Xu, Liping Guan, Xueshan Xiao, et al.
Nature Communications|June 13, 2024
Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasiaWenmin Sun, Dan Xiong, Jiamin Ouyang, et al.
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