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Molecular Vision|January 27, 2009
Evaluation of MFRP as a candidate gene for high hyperopiaPanfeng Wang, Zhikuan Yang, Shiqiang Li, et al.
Molecular Vision|November 4, 2008
Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinismShaohua Fang, Xiangming Guo, Xiaoyun Jia, et al.
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.
Acta Ophthalmologica|July 6, 2019
RPE65 mutation frequency and phenotypic variation according to exome sequencing in a tertiary centre for genetic eye diseases in ChinaShiqiang Li, Xueshan Xiao, Zhen Yi, et al.
Molecular Vision|March 20, 2010
Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in ChineseYanli Ji, Xiaoyun Jia, 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.
Molecular Vision|January 6, 2012
Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amaurosis resulting from CRB1 mutationsLin Li, Xueshan Xiao, Shiqiang Li, et al.
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