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浏览/检索结果: 共13条，第1-10条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Causes of Visual Impairment and Blindness in the 2006 and 2014 Nine-Province Surveys in Rural China 期刊论文 AMERICAN JOURNAL OF OPHTHALMOLOGY, 2019, 卷号: 197 作者:  Zhao, Jialiang;  Xu, Xiao;  Ellwein, Leon B.;  Guan, Huaijin;  He, Mingguang 收藏  |  浏览/下载：36/0  |  提交时间：2019/12/04 Causes of Visual Impairment and Blindness in the 2006 and 2014 Nine-Province Surveys in Rural China 期刊论文 2019, 卷号: 197, 页码: 80-87 作者:  Zhao, Jialiang;  Xu, Xiao;  Ellwein, Leon B.;  Guan, Huaijin;  He, Mingguang 收藏  |  浏览/下载：30/0  |  提交时间：2020/01/03 IFT52 as a Novel Candidate for Ciliopathies Involving Retinal Degeneration 期刊论文 INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2018, 卷号: 59, 期号: 11 作者:  Chen, Xue;  Wang, Xiaoguang;  Jiang, Chao;  Xu, Min;  Liu, Yang 收藏  |  浏览/下载：9/0  |  提交时间：2019/12/05 Liber congenital amaurosis  ciliopathy  IFT52 gene  mutation  cellular study   Distinct mutations with different inheritance mode caused similar retinal dystrophies in one family: a demonstration of the importance of genetic annotations in complicated pedigrees 期刊论文 JOURNAL OF TRANSLATIONAL MEDICINE, 2018, 卷号: 16 作者:  Chen, Xue;  Sheng, Xunlun;  Liu, Yani;  Li, Zili;  Sun, Xiantao 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/05 Retinitis pigmentosa  Genetic heterogeneity  Next generation sequencing  Mutation  OFDI  C8ORF37  TULP1  RP1  Consanguinity   Cataract Surgical Coverage and Visual Acuity Outcomes in Rural China in 2014 and Comparisons With the 2006 China Nine-Province Survey 期刊论文 2018, 卷号: 193, 页码: 62-70 作者:  Zhao, Jialiang;  Xu, Xiao;  Ellwein, Leon B.;  Guan, Huaijin;  He, Mingguang 收藏  |  浏览/下载：17/0  |  提交时间：2020/01/03 Prevalence of Vision Impairment in Older Adults in Rural China in 2014 and Comparisons With the 2006 China Nine-Province Survey 期刊论文 2018, 卷号: 185, 页码: 81-93 作者:  Zhao, Jialiang;  Xu, Xiao;  Ellwein, Leon B.;  Cai, Ning;  Guan, Huaijin 收藏  |  浏览/下载：10/0  |  提交时间：2020/01/03 Blindness  Population-based survey  Rural China  Vision impairment   CEP78 is mutated in a distinct type of Usher syndrome 期刊论文 JOURNAL OF MEDICAL GENETICS, 2017, 卷号: 54, 期号: 3 作者:  Fu, Qing;  Xu, Mingchu;  Chen, Xue;  Sheng, Xunlun;  Yuan, Zhisheng 收藏  |  浏览/下载：8/0  |  提交时间：2019/12/05 GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity 期刊论文 GENETICS IN MEDICINE, 2017, 卷号: 19, 期号: 8 作者:  Chen, Xue;  Sheng, Xunlun;  Zhuang, Wenjuan;  Sun, Xiantao;  Liu, Guohua 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/05 GUCA1A  maculopathy  medical genetics  ophthalmology  pathogenic mechanism   GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity 期刊论文 GENETICS IN MEDICINE, 2017, 卷号: 19, 期号: 8, 页码: 945-954 作者:  Chen, Xue;  Sheng, Xunlun;  Zhuang, Wenjuan;  Sun, Xiantao;  Liu, Guohua 收藏  |  浏览/下载：10/0  |  提交时间：2019/12/12 GUCA1A  maculopathy  medical genetics  ophthalmology  pathogenic  mechanism   CEP78 is mutated in a distinct type of Usher syndrome 期刊论文 2017, 卷号: 54, 期号: 3, 页码: 190-195 作者:  Fu, Qing;  Xu, Mingchu;  Chen, Xue;  Sheng, Xunlun;  Yuan, Zhisheng 收藏  |  浏览/下载：4/0  |  提交时间：2020/01/04 CEP78  Usher syndrome  cone-rod dystrophy  next-generation sequencing