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Investigative Ophthalmology & Visual Science|August 16, 2012
PAX6 mutations identified in 4 of 35 families with microcorneaPanfeng Wang, Wenmin Sun, Shiqiang Li, et al.Molecular Vision|June 21, 2006
Novel mutations of the PAX6 gene identified in Chinese patients with aniridiaPanfeng Wang, Xiangming Guo, Xiaoyun Jia, et al.Global Spine Journal|April 13, 2021
An Effective Surgical Method for Terminal Syringomyelia: Terminal Ventriculostomy-Associated "V"-Type OstomyMengchun Sun, Benzhang Tao, Gan Gao, et al.Physics in Medicine and Biology|May 24, 2024
Mechanism of acoustic pressure spectrum shifting toward lower frequencies in applied current thermoacoustic imagingWenwei Zhang, Hui Xia, Xiaonan Li, et al.Ebiomedicine|May 27, 2020
Comparative exome sequencing reveals novel candidate genes for retinitis pigmentosaZhen Yi, Jiamin Ouyang, Wenmin Sun, et al.Plos One|January 13, 2017
Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic NeuropathyYadi Li, Jie Li, Xiaoyun Jia, et al.Molecular Medicine Reports|March 25, 2017
GPR143 mutations in Chinese patients with ocular albinism type 1Xiuhua Jia, Jin Yuan, Xiaoyun Jia, et al.Molecular Vision|August 19, 2011
Mutation spectrum of PAX6 in Chinese patients with aniridiaXiaohui Zhang, Panfeng Wang, Shiqiang Li, et al.Molecular Medicine Reports|June 29, 2017
Novel mutations of FRMD7 in Chinese patients with congenital motor nystagmusXiuhua Jia, Xiang Zhu, Qigen Li, et al.Journal of Human Genetics|October 22, 2005
Linkage analysis of two families with X-linked recessive congenital motor nystagmusXiangming Guo, Shiqiang Li, Xiaoyun Jia, et al.Pageof 22