机构

• 广州生物医药与健康研... [4]

采集方式

• OAI收割 [4]

内容类型

• 期刊论文 [4]

发表日期

• 2016 [4]

学科主题

• Pediatrics [2]
• Psychiatry [2]

筛选

浏览/检索结果: 共4条，第1-4条 帮助 限定条件 存缴方式：oaiharvest    发表日期：2016    专题：广州生物医药与健康研究院    第一署名单位    第一作者单位    通讯作者单位     条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择提交时间升序提交时间降序发表日期升序发表日期降序题名升序题名降序作者升序作者降序 CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation 期刊论文  OAI收割 TRANSLATIONAL PSYCHIATRY, 2016, 卷号: 6 Liu, J.; Gao, C.; Chen, W.; Ma, W.; Li, X.; Shi, Y.; Zhang, H.; Zhang, L.; Long, Y.; Xu, H.; Guo, X.; Deng, S.; Yan, X.; Yu, D.; Pan, G.; Chen, Y.; Lai, L.; Liao, W.; Li, Z. 收藏  |  浏览/下载：31/0  |  提交时间：2016/12/16 Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations 期刊论文  OAI收割 JOURNAL OF PEDIATRICS, 2016, 卷号: 174 作者:  Liu, Ting;  Li, Fucheng;  Yue, Zhihui;  Xu, Tingting;  Chen, Minghui   |  收藏  |  浏览/下载：44/0  |  提交时间：2018/12/13 CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation 期刊论文  OAI收割 TRANSLATIONAL PSYCHIATRY, 2016, 卷号: 6 作者:  Li, Z.;  Liu, J.;  Gao, C.;  Chen, W.;  Ma, W.   |  收藏  |  浏览/下载：16/0  |  提交时间：2018/12/13 Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations 期刊论文  OAI收割 JOURNAL OF PEDIATRICS, 2016, 卷号: 174 Li, Fucheng; Yue, Zhihui; Xu, Tingting; Chen, Minghui; Zhong, Liangying; Liu, Ting; Jing, Xiangyi; Deng, Jia; Hu, Bin; Liu, Yuling; Wang, Haiyan; Lai, Kar N.; Sun, Liangzhong; Liu, Jinsong; Maxwell, Patrick H.; Wang, Yiming 收藏  |  浏览/下载：43/0  |  提交时间：2016/12/16