卵母细胞成熟障碍的致病基因定位研究
序号 | 标题 | 类型 | 作者 |
---|---|---|---|
1 | A Genome-wide Association Study Reveals that Variants within the HLA Region Are Associated with Risk for Nonobstructive Azoospermia | 期刊论文 | Qin Y|Xu J|Zhang H|Sun J|Sun Y|Wang Z|Liu J|Ding Q|Lu S| |
2 | Identification of YAP1 as a novel susceptibility gene for polycystic ovary syndrome | 期刊论文 | Li T|Zhao H|Zhao X|Zhang B|Cui L|Shi Y|Li G|Wang P|Chen ZJ| |
3 | Association Study of Gene LPP in Women with Polycystic Ovary Syndrome. | 期刊论文 | Zhang B|Zhao H|Li T|Gao X|Gao Q|Tang R|Zhang J|Chen ZJ| |
4 | Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome | 期刊论文 | Shi Y|Zhao H|Shi Y|Cao Y|Yang D|Li Z|Zhang B|Liang X| |
5 | Variants in DENND1A and LHCGR are associated with endometrioid adenocarcinoma. | 期刊论文 | Wang Z|Li T|Zhang W|You L|Zhao Y|Xia M|Zhao H|Chen ZJ| |
6 | Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3. | 期刊论文 | Zhao H|Xu X|Xing X|Wang J|He L|Shi Y|Zhao Y|Chen ZJ| |