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American Journal of Medical Genetics. Part A|July 18, 2009
Iris hyperpigmentation in a Chinese family with ocular albinism and the GPR143 mutationXueshan Xiao, Qingjiong Zhang
Ophthalmic Genetics|December 17, 2011
Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutationXueshan Xiao, Shiqiang Li, Qingjiong Zhang
Human Genetics|November 9, 2011
A novel locus for autosomal dominant congenital motor nystagmus mapped to 1q31-q32.2 between D1S2816 and D1S2692Xueshan Xiao, Shiqiang Li, Xiangming Guo, et al.
Materials (Basel, Switzerland)|January 11, 2025
The Effects of Nitrogen Alloying on the Microstructure and Properties of Cu-Bearing Antimicrobial Stainless SteelYuguo Tu, Wei Peng, Liujie Chen, et al.
Molecular Vision|September 5, 2007
FRMD7 mutations in Chinese families with X-linked congenital motor nystagmusQingjiong Zhang, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|February 11, 2009
Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopiaZhikuan Yang, Xueshan Xiao, Shiqiang Li, et al.
International Journal of Molecular Medicine|August 2, 2011
KIF21A novel deletion and recurrent mutation in patients with congenital fibrosis of the extraocular muscles-1Panfeng Wang, Shiqiang Li, Xueshan Xiao, et al.
Biochemical and Biophysical Research Communications|May 14, 2011
Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophyXueshan Xiao, Guiying Mai, Shiqiang Li, et al.
Molecular Vision|January 8, 2020
Spectrum, frequency, and genotype-phenotype of mutations in <i>SPATA7</i>Xueshan Xiao, Wenmin Sun, Shiqiang Li, et al.
Experimental Eye Research|October 19, 2019
Pathogenicity discrimination and genetic test reference for CRX variants based on genotype-phenotype analysisZhen Yi, Xueshan Xiao, Shiqiang Li, et al.
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