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Molecular Vision|July 29, 2010
PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1Juan Wang, Shiqiang Li, Xueshan Xiao, et al.
Molecular Medicine Reports|October 14, 2011
High myopia is not associated with single nucleotide polymorphisms in the COL2A1 gene in the Chinese populationJuan Wang, Panfeng Wang, Yang Gao, et al.
Eye (London, England)|November 27, 2021
Clinical features and genetic spectrum of NMNAT1-associated retinal degenerationZhen Yi, Shiqiang Li, Siyu Wang, et al.
Frontiers in Cell and Developmental Biology|March 8, 2021
Dominant RP in the Middle While Recessive in Both the N- and C-Terminals Due to <i>RP1</i> Truncations: Confirmation, Refinement, and QuestionsJunwen Wang, Xueshan Xiao, Shiqiang Li, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 28, 2021
Pathogenic variants and associated phenotypic spectrum of TSPAN12 based on data from a large cohortWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 10, 2010
Nonsyndromic high myopia in a Chinese family mapped to MYP1: linkage confirmation and phenotypic characterizationXiangming Guo, Xueshan Xiao, Shiqiang Li, et al.
Spine|October 26, 2019
Anterior Sacral Meningocele: A New Classification and Treatment Using the Dorsal Transsacral ApproachCheng Cheng, Benzhang Tao, Shaocong Bai, et al.
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