CORC

浏览/检索结果: 共55条,第1-10条 帮助

限定条件                    
已选(0)清除 条数/页:   排序方式:
Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract 期刊论文
MOLECULAR GENETICS AND GENOMICS, 2019, 卷号: 294, 期号: 2
作者:  Yang, Nan;  Song, Chengcheng;  Xu, Hong;  Zhang, Feng;  Wang, Hongyan
收藏  |  浏览/下载:34/0  |  提交时间:2019/12/05
Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella 期刊论文
JOURNAL OF MEDICAL GENETICS, 2019, 卷号: 56, 期号: 2
作者:  He, Xiaojin;  Li, Weiyu;  Wu, Huan;  Lv, Mingrong;  Liu, Wangjie
收藏  |  浏览/下载:41/0  |  提交时间:2019/12/05
Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia 期刊论文
JOURNAL OF GENETICS AND GENOMICS, 2019, 卷号: 46, 期号: 1
作者:  Liu, Wangjie;  Wu, Huan;  Wang, Li;  Yang, Xiaoyu;  Liu, Chunyu
收藏  |  浏览/下载:40/0  |  提交时间:2019/12/05
Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility 期刊论文
JOURNAL OF HUMAN GENETICS, 2019, 卷号: 64, 期号: 1
作者:  Li, Weiyu;  He, Xiaojin;  Yang, Shenmin;  Liu, Chunyu;  Wu, Huan
收藏  |  浏览/下载:30/0  |  提交时间:2019/12/05
An episomal vector-based CRISPR/Cas9 system for highly efficient gene knockout in human pluripotent stem cells (vol 7, 2320, 2018) 期刊论文
SCIENTIFIC REPORTS, 2018, 卷号: 8
作者:  Xie, Yifang;  Wang, Daqi;  Lan, Feng;  Wei, Gang;  Ni, Ting
收藏  |  浏览/下载:16/0  |  提交时间:2019/12/05
Database Resources of the BIG Data Center in 2018 期刊论文
NUCLEIC ACIDS RESEARCH, 2018, 卷号: 46, 期号: D1
作者:  Xu, Xingjian;  Hao, Lili;  Zhu, Junwei;  Zhou, Qing;  Song, Fuhai
收藏  |  浏览/下载:54/0  |  提交时间:2019/12/05
2018 Chinese Pediatric Cardiology Society (CPCS) guideline for diagnosis and treatment of syncope in children and adolescents 期刊论文
SCIENCE BULLETIN, 2018, 卷号: 63, 期号: 23
作者:  Li, Tao;  Wang, Cheng;  Li, Yaqi;  Liao, Ying;  Tian, Hong
收藏  |  浏览/下载:53/0  |  提交时间:2019/12/05
Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders 期刊论文
HUMAN MOLECULAR GENETICS, 2017, 卷号: 26, 期号: 10
作者:  Jiang, Yuwu;  Wang, Jingmin;  Zhang, Cheng;  Li, Dongxiao;  Ji, Haoran
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/05
A novel BMX variant promotes tumor cell growth and migration in lung adenocarcinoma 期刊论文
ONCOTARGET, 2017, 卷号: 8, 期号: 20
作者:  Wang, Ye;  Xia, Jufeng;  Fang, Zhaoyuan;  Li, Fei;  Li, Duo
收藏  |  浏览/下载:5/0  |  提交时间:2019/12/05
Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella 期刊论文
AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 卷号: 100, 期号: 6
作者:  Tang, Shuyan;  Wang, Xiong;  Li, Weiyu;  Yang, Xiaoyu;  Li, Zheng
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/05


©版权所有 ©2017 CSpace - Powered by CSpace