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The Bethesda System for Reporting Thyroid Cytopathology(TBSRTC):A report of 2,781 cases in a Chinese
[期刊论文] 作者:Yanli Zhu,Yuntao Song,Guohui X,
来源:中国癌症研究:英文版 年份:2020
Objective:To evaluate the diagnostic utility of The Bethesda System for Reporting Thyroid Cytology(TBSRTC)at Peking University Cancer Hospital,the incidence of...
Anti-tumor effect of the extract from Qingyihuaji formula on pancreatic cancer by down-regulating No
[期刊论文] 作者:Xu Yanli,Zhu Feiye,Xu Shan,Liu Luming,
来源:中医杂志(英文版) 年份:2015
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Anti-tumor effect of the extract from Qingyihuaji formula on pancreatic cancer by down-regulating No
[期刊论文] 作者:Xu Yanli,Zhu Feiye,Xu Shan,Liu L,
来源:Journal of Traditional Chinese M 年份:2020
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[期刊论文] 作者:Wang Yao,Wen Guangjun,Mao Wei,He Yanli,Zhu Xueyong,
来源:城市道桥与防洪 年份:2011
该文从挂篮荷载计算、施工流程、支座及临时固结施工、挂篮安装及试验、合拢段施工、模板制作安装、钢筋安装、混凝土的浇筑及养生、测量监控等方面人手,介绍了S226海滨大桥...
Virtual bronchoscopic navigation without fluoroscopy guidance for peripheral pulmonary lesions in in
[期刊论文] 作者:Shijie Li,Wanpu Yan,Mailin Chen,Zhongwu Li,Yanli Zhu,Qi Wu,
来源:中国癌症研究(英文版) 年份:2020
Objective: Fluoroscopy guidance is generally required for endobronchial ultrasonography with guide sheath (EBUS-GS) in peripheral pulmonary lesions (PPLs).Virtu...
[会议论文] 作者:Guikuan Yue,Yanli Zhu,Xingmei Lv,Hongyan He,Shucai Li,Suojiang Zhang,
来源:中国国际绿色化学研讨会(The 8th International Symposium on Green Chemist 年份:2007
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Genetic Variation of the VP1 Gene of the Virulent Duck Hepatitis A Virus Type 1 (DHAV-1) Isolates in
[期刊论文] 作者:Jiming Gao,Junhao Chen,Xingkui Si,Zhijing Xie,Yanli Zhu,Xingxiao Zhang,Shujing Wang,Shijin Jiang,
来源:中国病毒学 年份:2012
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Subtle Mutation detection of SMN1 gene in Chinese SMA Patients:implication of Molecular Diagnostic P
[会议论文] 作者:JinLi Bai,YuJin Qu,YanYan Cao,Yan Li,WenHui Zhang,YuWei Jin,Hong Wang,Fang Song,EeZhen Li,LiWen Wang,YanLi Zhu,
来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
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Subtle Mutation detection of SMN1 gene in Chinese SMA Patients:implication of Molecular Diagnostic P
[会议论文] 作者:JinLi Bai,YuJin Qu,YanYan Cao,EeZhen Li,LiWen Wang,Yan Li,YanLi Zhu,WenHui Zhang,YuWei Jin,Hong Wang,,
来源:2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份:2014
Background: Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder, which is caused by mutations of survival motor neuron 1 (SMN1) gene.Approximately 90-95% of SMA patien...
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