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SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis. 期刊论文
Genetics in medicine : official journal of the American College of Medical Genetics, 2019, 卷号: 21, 期号: 11, 页码: 2577-2585
作者:  Yang, Yongjia*;  Zheng, Yu;  Li, Wangming;  Li, Liping;  Tu, Ming
收藏  |  浏览/下载:5/0  |  提交时间:2019/12/27
Identification and characterization of NF1 and non-NF1 congenital pseudarthrosis of the tibia based on germline NF1 variants: genetic and clinical analysis of 75 patients. 期刊论文
Orphanet journal of rare diseases, 2019, 卷号: 14, 期号: 1, 页码: 221
作者:  Zhu, Guanghui;  Zheng, Yu;  Liu, Yaoxi;  Yan, An;  Hu, Zhengmao
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/27
The copy number of Epstein-Barr virus latent genome correlates with the oncogenicity by the activation level of LMP1 and NF-kappaB. 期刊论文
Oncotarget, 2015, 卷号: 6, 期号: 38, 页码: 41033-41044
作者:  Zuo, Lielian
收藏  |  浏览/下载:5/0  |  提交时间:2019/12/27
Prohibitin is an important biomarker for nasopharyngeal carcinoma progression and prognosis 期刊论文
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP), 2013, 卷号: 22, 期号: 1, 页码: 68-76
作者:  Liao, Qianjin;  Guo, Xiaofang;  Li, Xiaoling;  Xiong, Wei;  Li, Xiayu
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/27
游泳联合抚触护理降低新生儿黄疸的效果观察 期刊论文
南华大学学报(医学版), 2010, 期号: 01, 页码: 140-141+146
作者:  于小华;  张自珍;  黄海波;  王芳;  张平
收藏  |  浏览/下载:1/0  |  提交时间:2019/12/27


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