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浏览/检索结果: 共6条，第1-6条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择发表日期升序发表日期降序作者升序作者降序提交时间升序提交时间降序题名升序题名降序 Prognostic Value of Preoperative Systemic Immune-Inflammation Index in Patients with Cervical Cancer 期刊论文 SCIENTIFIC REPORTS, 2019, 卷号: 9, 期号: 1, 页码: 3284 作者:  Huang, Huaping[1];  Liu, Qin[2];  Zhu, Lixia[3];  Zhang, Yan[4];  Lu, Xiaojuan[5] 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/24 Controlled Synthesis and Photocatalytic Performance of Au@ZnO Nanospheres with Core-Shell and Yolk-Shell Structures Assisted by Carbonaceous Layers as Intermediate 期刊论文 Journal of nanoscience and nanotechnology, 2018, 卷号: 18, 页码: 2555-2561 作者:  Chen Lixia[1];  Peng Yiting[2];  He Fang[3];  Liu Guigao[4];  Huang Yuan[5] 收藏  |  浏览/下载：2/0  |  提交时间：2019/04/24 A rare case of B-lymphoproliferative disorder with villous lymphocytes harboring t(8;14)(q24;q32) translocation 期刊论文 FRONTIERS OF MEDICINE, 2018, 卷号: 12, 期号: 3, 页码: 324-329 作者:  Shi, Xiaofeng[1];  Ba, Rong[2];  You, Haiyan[3];  Jiang, Qian[4];  Huang, Jiansong[5] 收藏  |  浏览/下载：14/0  |  提交时间：2019/12/24 splenic lymphoma with villous lymphocytes  splenic marginal zone lymphoma  transformation  chromosome translocation   Dynamic analysis of localized defects in rolling bearing systems 会议论文 28th International Conference on Vibroengineering, 2017-10-19 作者:  Song, Mengmeng[1];  Xiao, Shungen[2];  Huang, Lixia[3];  Li, Wanxiang[4] 收藏  |  浏览/下载：2/0  |  提交时间：2019/04/24 Dynamic analysis of reciprocating compressor system with translational clearance and time-varying load 会议论文 30th International Conference on Vibroengineering, 2017-12-16 作者:  Song, Mengmeng[1];  Xiao, Shungen[2];  Song, Haixia[3];  Huang, Lixia[4] 收藏  |  浏览/下载：3/0  |  提交时间：2019/04/24 C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients 期刊论文 MOLECULAR MEDICINE REPORTS, 2017, 卷号: 16, 页码: 5333-5337 作者:  Lin, Ying[1];  Gao, Hongbin[2,3];  Ai, Siming[1];  Eswarakumar, Jacob V. P.[4];  Chen, Chuan[1,5] 收藏  |  浏览/下载：2/0  |  提交时间：2019/04/24 craniosynostosis  fibroblast growth factor receptor 2  gene  mutation  Peters anomaly  Pfeiffer syndrome  Crouzon syndrome