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
发布时间:2020-01-14
点击次数:
影响因子:2.695
发表刊物:Mol Genet Genomic Med
合写作者:Tan YQ*, Du J, Lin G, Lu GX, Zhong CG, Li XR, Li W, Gong F, He WB, Yang XW
文献类型:J
卷号:6
期号:2
页面范围:261-267
是否译文:否
发表时间:2018-03-01
收录刊物:SCI
上一条: He WB, Du J, Yang XW, Li W, Tang WL, Dai C, Chen YZ, Zhang YX, Lu GX, Lin G, Gong F, Tan YQ*. Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome
下一条: 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