Congenital Short-Bowel Syndrome Is Associated With a Novel Deletion Mutation in the CLMP Gene: Mutations in CLMP Caused CSBS

por Ou, Fen-fen, Li, Ming-jie, Mei, Li-bin, Lin, Xin-Zhu, Wu, Yan-an
Publicado 2022

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint

por Sha, Yan-Wei, Mei, Li-Bin, Zheng, Liang-Kai, Tian, Rui-Hua, Ding, Lu, Ji, Zhi-Yong, Zhang, Qing, Li, Ping
Publicado 2018

Sperm-egg fusion disorder in a Chinese male patient was associated with a rare ADAM20 variant

por Sha, Yan-Wei, Xu, Xiaohui, Ji, Zhi-Yong, Mei, Li-Bin, Qiu, Ping-Ping, Ji, Hong, Li, Ping, Li, Lin, Liu, Wei-Wu
Publicado 2017

Novel IFT140 variants cause spermatogenic dysfunction in humans

por Wang, Xiong, Sha, Yan‐wei, Wang, Wen‐ting, Cui, Yuan‐qing, Chen, Jie, Yan, Wei, Hou, Xiao‐tao, Mei, Li‐bin, Yu, Cui‐cui, Wang, Jiahui
Publicado 2019