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
发布时间:2020-01-14
点击次数:
影响因子:1.506
发表刊物:Mol Cytogenet
合写作者:Tan YQ*, Lu G, Lin G, Luo A, Meng L, Tu C, Yuan S, Xiong B, Yi D, He W, Cheng D, Li W, Du J, Li H
文献类型:J
卷号:11
页面范围:15
是否译文:否
发表时间:2018-02-05
收录刊物:SCI
上一条: Yang XW, He WB, Gong F, Li W, Li XR, Zhong CG, Lu GX, Lin G, Du J, Tan YQ*. Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiency
下一条: 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