He WB, Du J, Xie PY, Zhou S, Zhang YX, Lu GX, Lin G, Li W, Tan YQ*. X-chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations
发布时间:2020-01-14
点击次数:
影响因子:3.043
发表刊物:Prenat Diagn
合写作者:Tan YQ*, Li W, Lin G, Lu GX, Zhang YX, Zhou S, Xie PY, Du J, He WB
文献类型:J
卷号:39
期号:8
页面范围:603-608
是否译文:否
发表时间:2019-07-02
收录刊物:SCI
上一条: Xiao WJ, He WB, Zhang YX, Meng LL, Lu GX, Lin G, Tan YQ*, Du J*. In-Frame variants in STAG3 gene cause premature ovarian insufficiency
下一条: 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