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浏览/检索结果: 共8条，第1-8条 帮助 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 Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death 期刊论文 2018, 卷号: 51, 期号: 2, 页码: 309 作者:  Lin, Yubi[1];  He, Siqi[1,2];  Liao, Zili[1];  Feng, Ruiling[1,2];  Liu, Ruilin[3] 收藏  |  浏览/下载：10/0  |  提交时间：2019/12/17 Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles 期刊论文 2017, 卷号: 138, 期号: 1, 页码: 41 作者:  Lin, Yubi[1,2];  Zhang, Qianhuan[1];  Zhong, Zhi An[1];  Xu, Zhe[3];  He, Siqi[1,2] 收藏  |  浏览/下载：17/0  |  提交时间：2019/12/06 The Electrochemical Behavior of Nafion/Reduced Graphene Oxide Modified Carbon Electrode Surface and Its Application To Ascorbic Acid Determination 期刊论文 2015, 卷号: 10, 页码: 5747-5755 作者:  Liao, Wenli[1];  Guo, Chaozhong[1,2];  Sun, Lingtao[2];  Li, Zhongbin[1];  Tian, Liangliang[2] 收藏  |  浏览/下载：2/0  |  提交时间：2019/11/30 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：2/0  |  提交时间：2019/04/11 SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syn (CPCI-S收录) 会议 作者:  Lin, Yubi[1,2];  Deng, Chunyu[1,2];  Zhan, XianZhang[1,2];  Xu, Zhe[3];  Zhu, Jiening[1,2] 收藏  |  浏览/下载：11/0  |  提交时间：2019/04/11 The clinical characteristics of idiopathic outflow ventricular arrhythmias (CPCI-S收录) 会议 作者:  Qiu, Jia[1];  Xue, Yumei[1];  Liao, Zili[1] 收藏  |  浏览/下载：1/0  |  提交时间：2019/04/11 Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death 会议论文 Beijing, PEOPLES R CHINA, OCT 12-15, 2017 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：7/0  |  提交时间：2019/12/13 SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syndrome, and Progressive Conduction Disease 会议论文 Beijing, PEOPLES R CHINA, OCT 12-15, 2017 作者:  Lin, Yubi[1,2];  Deng, Chunyu[1,2];  Zhan, XianZhang[1,2];  Xu, Zhe[3];  Zhu, Jiening[1,2] 收藏  |  浏览/下载：13/0  |  提交时间：2019/12/10