QQ客服 官方微博 反馈留言

浏览/检索结果: 共3条，第1-3条 帮助 限定条件 学科主题：Science & Technology - Other Topics     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 Quantitative assessment of single-cell whole genome amplification methods for detecting copy number variation using hippocampal neurons 期刊论文 SCIENTIFIC REPORTS, 2015, 卷号: 5 作者:  Tong, Yin;  Zhang, Meng;  Chen, Yao;  Qin, Li;  Chen, Xiaoping 收藏  |  浏览/下载：14/0  |  提交时间：2018/12/13 Quantitative assessment of single-cell whole genome amplification methods for detecting copy number variation using hippocampal neurons 期刊论文 SCIENTIFIC REPORTS, 2015, 卷号: 5 Ning, Luwen; Li, Zhoufang; Wang, Guan; Hu, Wen; Hou, Qingming; Tong, Yin; Zhang, Meng; Chen, Yao; Qin, Li; Chen, Xiaoping; Man, Heng-Ye; Liu, Pinghua; He, Jiankui 收藏  |  浏览/下载：34/0  |  提交时间：2016/12/16 High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability 期刊论文 PLOS ONE, 2012, 卷号: 7, 期号: 4, 页码: -e34739 Gong, XH; Jiang, YW; Zhang, X; An, Y; Zhang, J; Wu, Y; Wang, JM; Sun, YF; Liu, YY; Gao, XW; Shen, YP; Wu, XR; Qiu, ZL; Jin, L; Wu, BL; Wang, HY 收藏  |  浏览/下载：19/0  |  提交时间：2013/06/04 SCAFFOLDING PROTEIN SHANK3  COPY NUMBER VARIATION  MENTAL-RETARDATION  CONGENITAL-ANOMALIES  LEARNING-DISABILITY  GENE-EXPRESSION  ARRAY CGH  DELAY