Zhang YX, Li HY, He WB, Tu C, Du J, Li W, Lu GX, Lin G, Yang Y, Tan YQ*. XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans
发布时间:2020-01-14
点击次数:
影响因子:4.104
发表刊物:Clin Genet
合写作者:Tan YQ*, Yang Y, Lin G, Lu GX, Li W, Du J, Tu C, He WB, Li HY, Zhang YX
文献类型:J
卷号:95
期号:3
页面范围:442-443
是否译文:否
发表时间:2019-03-01
收录刊物:SCI
上一条: Tan YQ, Tu CF, Meng LL, Yuan SM, Sjaarda C, Luo AX, Du J, Li W, Gong F, Zhong CG, Deng HX, Lu GX, Liang P, Lin G. Loss-of-function mutations TDRD7 lead to a rare novel syndrome combining congenital cataract and non-obstructive azoospermia in humans
下一条: Meng LL, Yuan SM, Tu CF, Lin G, Lu GX, Tan YQ*. Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China