He WB, Banerjee S, Meng LL, Du J, Gong F, Huang H, Zhang XX, Wang YY, Lu GX, Lin G, Tan YQ*. Whole-exome sequencing identifies a homozygous donor splice-site mutation in STAG3 that causes primary ovarian insufficiency
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*, Lin G, Lu GX, Wang YY, Zhang XX, Huang H, Gong F, Du J, Meng LL, Banerjee S, He WB
文献类型：J
卷号：93
期号：2
页面范围：340-344
是否译文：否
发表时间：2018-02-01
收录刊物：SCI
上一条： Li H, Du J, Li W, Cheng D, He W, Yi D, Xiong B, Yuan S, Tu C, Meng L, Luo A, Lin G, Lu G, Tan YQ*. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature
下一条： He WB, Tan YQ, Hu X, Li W, Xiong B, Luo KL, Gong F, Lu GX, Lin G, Du J. Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency