Xu F, Zhang YN, Cheng DH, Tan K, Zhong CG, Lu GX, Lin G, Tan YQ*. The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes
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*, Lin G, Lu GX, Zhong CG, Tan K, Cheng DH, Zhang YN, Xu F
文献类型：J
卷号：7
期号：1
页面范围：64-69
是否译文：否
发表时间：2014-10-03
收录刊物：SCI
上一条： 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
下一条： Wang W, Tu C, Nie H, Meng L, Li Y, Yuan S, Zhang Q, Du J, Wang J, Gong F, Fan L, Lu GX, Lin G, Tan YQ*. Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations