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Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in the southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G > A 会议论文
作者:  Wang, Zhi-Qiang;  Chen, Xue-Jiao;  Murong, Shen-Xing;  Wang, Ning;  Wu, Zhi-Ying
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/19
A clinical study of prevalence and Characteristics of the Metabolic Syndrome in Primary Aldosteronism 会议论文
作者:  Jing Jing;  Xiaomu Li;  Jian GAO;  Chen Chen;  Zhi Qiang LU
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/19
Establishment of a core fucosylated glycoprotein profile from normal liver tissues using LCA chromatography followed by MALDI-TOF-MS/MS 会议论文
作者:  Dai, Zhi;  Guo, Kun;  Sun, Qiang-Ling;  Lu, Wen-Jing;  Zhou, Hai-Jun
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/27


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