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浏览/检索结果: 共6条，第1-6条 帮助 限定条件 内容类型：会议     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 Familial Sudden Cardiac Death Caused by DSG2 Mutation as Genetic Backgrounds: Whole Exome Sequencing and Valid Therapy of Catheter Ablation (CPCI-S收录) 会议 作者:  Lin, Yubi[1,2,3,4,5,6,7];  Zhang, Qianhuan[1,2,3,4,5,6];  Chen, Jia[8];  Feng, Ruiling[1,2,3,4,5,6,7];  He, Siqi[1,2,3,4,5,6,7] 收藏  |  浏览/下载：8/0  |  提交时间：2019/04/11 Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death (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 Differential Evolution with Random Walk Mutation and an External Archive for Multimodal Optimization (CPCI-S收录) 会议 作者:  Zhang, Yu-Hui;  Li, Meng-Ting;  Gong, Yue-Jiao[1];  Zhang, Jun 收藏  |  浏览/下载：1/0  |  提交时间：2019/04/11 A novel preimplantation genetic diagnosis method for monogenic diseases by targeted sequencing (CPCI-S收录) 会议 作者:  Li, J.[1];  Zhang, X. D.[1];  Xu, Y. W.[2];  Liu, S. J.[1];  Huang, Y. L.[1] 收藏  |  浏览/下载：10/0  |  提交时间：2019/04/11 preimplantation genetic diagnosis (PGD)  targeted sequencing  massively parallel sequencing (MPS)  haplotype linkage analysis  direct mutation detection   Association of the RUNX1/AML1 Gene Mutation and Familial MDS/AML: A Case Report and Review of Literature (CPCI-S收录) 会议 作者:  Chen, Wancheng[1];  Li, Hongbo[2] 收藏  |  浏览/下载：7/0  |  提交时间：2019/04/11 DECLINED PRESENTATION V beta 17 T CELL CLONES MAY RESPOND TO ABL-T315I MUTATION PROTEIN IN CHRONIC MYELOID LEUKEMIA IN BLASTIC CRISIS (CPCI-S收录) 会议 作者:  Xu, Ling[1];  Chen, Jie[2];  Zhang, Tao[2];  Zha, Xianfeng[2];  Chen, Shaohua[1] 收藏  |  浏览/下载：1/0  |  提交时间：2019/04/11