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Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa 期刊论文
HUMAN MOLECULAR GENETICS, 2018, 卷号: 27, 期号: 23
作者:  Zhang, Lin;  Sun, Zixi;  Zhao, Peiquan;  Huang, Lulin;  Xu, Mingchu
收藏  |  浏览/下载:22/0  |  提交时间:2019/12/05
New loci and coding variants confer risk for age-related macular degeneration in East Asians 期刊论文
NATURE COMMUNICATIONS, 2015, 卷号: 6
作者:  Cheng, Ching-Yu;  Yamashiro, Kenji;  Chen, Li Jia;  Ahn, Jeeyun;  Huang, Lulin
收藏  |  浏览/下载:20/0  |  提交时间:2019/12/13
Screening for Retinopathy of Prematurity in China: A Neonatal Units-Based Prospective Study 期刊论文
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2013, 卷号: 54, 期号: 13
作者:  Xu, Yu;  Zhou, Xiaohong;  Zhang, Qi;  Ji, Xunda;  Zhang, Qin
收藏  |  浏览/下载:5/0  |  提交时间:2019/12/19
Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population 期刊论文
AMERICAN JOURNAL OF HUMAN GENETICS, 2011, 卷号: 88, 期号: 6
作者:  Shi, Yi;  Qu, Jia;  Zhang, Dingding;  Zhao, Peiquan;  Zhang, Qingjiong
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/19
Comparison of electroretinogram between healthy preterm and term infants 期刊论文
DOCUMENTA OPHTHALMOLOGICA, 2010, 卷号: 121, 期号: 3
作者:  Zhou, Xiaohong;  Huang, Xin;  Chen, Hongling;  Zhao, Peiquan
收藏  |  浏览/下载:1/0  |  提交时间:2019/12/19


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