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Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death (CPCI-S收录) 会议
作者:  Lin, Yubi[1,2,3,4,5,6];  Liao, Zili[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Liu, Ruilin[7];  Peng, Yongzheng[8]
收藏  |  浏览/下载:3/0  |  提交时间:2019/04/11
The Quality Assessment of Clinical Teaching System Based on Legal Construction 会议
作者:  Hou, Kaijian[1];  Wang, Xuhuang[1];  Lin, Chuangjian[1];  Yao, Yinghua[1];  Wu, Bangtai[1]
收藏  |  浏览/下载:3/0  |  提交时间:2019/04/11


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