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Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency 期刊论文
2019, 卷号: 112, 期号: 3, 页码: 569-+
作者:  Zhou, Yiran;  Chen, Beili;  Li, Lin;  Pan, Hong;  Liu, Beihong
收藏  |  浏览/下载:4/0  |  提交时间:2020/01/03
CAPS Mutations Are Potentially Associated with Unexplained Recurrent Pregnancy Loss 期刊论文
2019, 卷号: 189, 期号: 1, 页码: 124-131
作者:  Pan, Hong;  Xiang, Huifen;  Wang, Jing;  Wei, Zhaolian;  Zhou, Yiran
收藏  |  浏览/下载:6/0  |  提交时间:2020/01/03
TNFRSF21 mutations cause high myopia 期刊论文
2019, 卷号: 56, 期号: 10, 页码: 671-677
作者:  Pan Hong;  Wu Shijing;  Wang Jing;  Zhu Tian;  Li Tengyan
收藏  |  浏览/下载:4/0  |  提交时间:2020/01/03
Carrying the T Allele of the SNP rs574344, an eQTL of GSTM1, Contributes to Longevity in the Han Chinese Population 期刊论文
2019, 卷号: 23, 期号: 1, 页码: 12-15
作者:  Zhang, Yunxia;  Zhang, Siyang;  Yan, Dongjing;  Pan, Hong;  Liu, Beihong
收藏  |  浏览/下载:11/0  |  提交时间:2020/01/03
longevity  Chinese  SNP  eQTL  GSTM1  


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