CORC

浏览/检索结果: 共12条,第1-10条 帮助

已选(0)清除 条数/页:   排序方式:
ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants 期刊论文
FRONTIERS IN GENETICS, 2019, 卷号: 10
作者:  Hu, Fang-Yuan;  Li, Jian-kang;  Gao, Feng-Juan;  Qi, Yu-He;  Xu, Ping
收藏  |  浏览/下载:50/0  |  提交时间:2019/12/05
Identification of a novel mutation in the ABCA4 gene in a Chinese family with retinitis pigmentosa using exome sequencing 期刊论文
Bioscience Reports, 2018, 卷号: 38, 期号: 2
作者:  Huang, Xiangjun;  Yuan, Lamei;  Xu, Hongbo;  Zheng, Wen;  Cao, Yanna
收藏  |  浏览/下载:11/0  |  提交时间:2019/12/27
Next-Generation Sequencing-Aided Rapid Molecular Diagnosis of Occult Macular Dystrophy in a Chinese Family 期刊论文
FRONTIERS IN GENETICS, 2017, 卷号: 8
作者:  Qi, Yu-He;  Gao, Feng-Juan;  Hu, Fang-Yuan;  Zhang, Sheng-Hai;  Chen, Jun-Yi
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/05
ABCA4基因相关视网膜变性类疾病的临床和基因研究 学位论文
: 北京协和医学院中国医学科学院;北京协和医学院;中国医学科学院;清华大学医学部, 2017
作者:  孙子系
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/04
Novel compound heterozygous mutations in ABCA4 in a Chinese pedigree with Stargardt disease 期刊论文
MOLECULAR VISION, 2016, 卷号: 22, 页码: 1514-1521
作者:  Zhang, Jianping[1];  Qi, Anhui[2,3];  Wang, Xi[3];  Pan, Hong[2,3];  Mo, Haiming[1]
收藏  |  浏览/下载:10/0  |  提交时间:2019/04/24
Novel compound heterozygous mutations in ABCA4 in a Chinese pedigree with Stargardt disease 期刊论文
2016, 卷号: 22, 页码: 1514-1521
作者:  Zhang, Jianping;  Qi, Anhui;  Wang, Xi;  Pan, Hong;  Mo, Haiming
收藏  |  浏览/下载:9/0  |  提交时间:2020/01/04
Associations of the G1961E and D2177N variants in ABCA4 and the risk of age-related macular degeneration 期刊论文
GENE, 2015, 卷号: 567, 期号: [db:dc_citation_issue], 页码: 51-57
作者:  Zhang, Rui;  Wang, Li-Yuan;  Wang, Ya-Feng;  Wu, Chang-Rui;  Lei, Chun-Ling
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/02
Correlation between the interactions of ABCA4 polymorphisms and smoking with the susceptibility to age-related macular degeneration 期刊论文
International Journal of Clinical and Experimental Pathology, 2015, 卷号: Vol.8 No.6, 页码: 7403–7408
作者:  Ying Wu;  Lei Tian;  Yifei Huang
收藏  |  浏览/下载:1/0  |  提交时间:2019/02/27
Exome sequencing analysis identifies compound heterozygous mutation in ABCA4 in a Chinese family with Stargardt disease 期刊论文
PLoS ONE, 2014, 卷号: 9, 期号: [db:dc_citation_issue]
作者:  Zhou, Yu;  Tao, Siyu;  Chen, Hui;  Huang, Lulin;  Zhu, Xiong
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/02
Exome Sequencing Analysis Identifies Compound Heterozygous Mutation in ABCA4 in a Chinese Family with Stargardt Disease 期刊论文
PLOS ONE, 2014, 卷号: 9, 期号: 3, 页码: e91962(1-8)
Zhou, Yu; Tao, Siyu; Chen, Hui; Huang, Lulin; Zhu, Xiong; Li, Youping; Wang, Zhili; Lin, He; Hao, Fang; Yang, Zhenglin; Wang, Liya; Zhu, Xianjun
收藏  |  浏览/下载:36/0  |  提交时间:2016/01/07


©版权所有 ©2017 CSpace - Powered by CSpace