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Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutations 期刊论文
2017, 卷号: 177, 期号: 4, 页码: 389-398
作者:  Nie, Min;  Xu, Hongli;  Chen, Rongrong;  Mao, Jiangfeng;  Wang, Xi
收藏  |  浏览/下载:3/0  |  提交时间:2020/01/03
HDL-cholesterol concentration in pregnant Chinese Han women of late second trimester associated with genetic variants in CETP, ABCA1, APOC3, and GALNT2 期刊论文
2017, 卷号: 8, 期号: 34, 页码: 56737-56746
作者:  Cui, Mingxuan;  Li, Wei;  Ma, Liangkun;  Ping, Fan;  Liu, Juntao
收藏  |  浏览/下载:13/0  |  提交时间:2020/01/04
Novel mutations of HSD17B3 in three Chinese patients with 46,XY Disorders of Sex Development 期刊论文
2017, 卷号: 126, 页码: 1-6
作者:  Yu Bingqing;  Liu Zhaoxiang;  Mao Jiangfeng;  Wang Xi;  Zheng Junjie
收藏  |  浏览/下载:3/0  |  提交时间:2020/01/03
Novel FSH beta mutation in a male patient with isolated FSH deficiency and infertility 期刊论文
2017, 卷号: 60, 期号: 6, 页码: 335-339
作者:  Zheng Junjie;  Mao Jiangfeng;  Cui Mingxuan;  Liu Zhaoxiang;  Wang Xi
收藏  |  浏览/下载:6/0  |  提交时间:2020/01/04
Pulsatile GnRH therapy may restore hypothalamus-pituitary-testis axis function in patients with congenital combined pituitary hormone deficiency: a prospective, self-controlled trial 期刊论文
2017, 卷号: 102, 期号: 7, 页码: 2291-2300
作者:  Zheng Junjie;  Mao Jangfeng;  Xu Hongli;  Wang Xi;  Huang Bingkun
收藏  |  浏览/下载:14/0  |  提交时间:2020/01/04
T2DM Self-Management via Smartphone Applications: A Systematic Review and Meta-Analysis 期刊论文
2016, 卷号: 11, 期号: 11, 页码: e0166718
作者:  Cui, Mingxuan;  Wu, Xueyan;  Mao, Jiangfeng;  Wang, Xi;  Nie, Min
收藏  |  浏览/下载:1/0  |  提交时间:2020/01/04


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