搜索筛选:
搜索耗时4.0009秒,为你在为你在102,285,761篇论文里面共找到 7 篇相符的论文内容
发布年度:
[期刊论文] 作者：Ma Yuwei Jin Zi,
来源：中关村 年份：2018
I remember a few years ago to participate in the social investigation organized by the Central Party School， the first stop is Guang'an in Sichuan Province， to the great hometown of Deng Xiaoping's ho...
[会议论文] 作者：Yanyan Cao,Yujin Qu,Jinli Bai,Yuwei Jin,Hong Wang,Fang Song,
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
...
[会议论文] 作者：JinLi Bai,YuJin Qu,YanYan Cao,Yan Li,WenHui Zhang,YuWei Jin,Hong Wang,Fang Song,
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
...
[期刊论文] 作者：Mengzhan Ge,Xiaodong Zhang,Shangzhou Xia,Wenjie Luo,Yuwei Jin,Qianqian Chen,Huagui Nie,Zhi Yang,
来源：中国化学（英文版） 年份：2021
Tremendous efforts have been made to the development of highly active,stable hydrogen evolution reaction(HER)electrocatalysts based on earth-abundant metal comp...
[会议论文] 作者：JinLi Bai,YuJin Qu,YanYan Cao,Yan Li,WenHui Zhang,YuWei Jin,Hong Wang,Fang Song,
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: Crigler-Najjar syndrome (CN-I) is a very rare autosomal recessive disease caused by the homozygous or compound heterozygous mutations of UPD-glucuronosyl-transferase 1A1 gene (UGT1A1) on c...
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,,
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
...
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...
相关搜索：
