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Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population 期刊论文
JOURNAL OF HUMAN GENETICS, 2015, 卷号: 60, 期号: 10, 页码: 625-630
作者:  Zhou, Yu;  Saikia, Bibhuti B.;  Jiang, Zhilin;  Zhu, Xiong;  Liu, Yuqing
收藏  |  浏览/下载:34/0  |  提交时间:2016/12/22
Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28 期刊论文
HUMAN MOLECULAR GENETICS, 2011, 卷号: 20, 期号: 16, 页码: 3213-3226
作者:  Du, Jiulin
收藏  |  浏览/下载:39/0  |  提交时间:2012/07/13
Mutation spectrum in Salmonella induced by environmental tobacco smoke 期刊论文
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1999, 卷号: 33, 期号: 3, 页码: 185-193
作者:  Zhou, RQ;  Yu, G;  Zhou, YQ;  Zeng, XF;  Zhou, RQ, Liaoning Univ, Dept Biol, Shenyang 110036, Liaoning Prov, Peoples R China
收藏  |  浏览/下载:74/0  |  提交时间:2011/09/23


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