A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review

por Sha, Yanwei, Zheng, Liangkai, Ji, Zhiyong, Mei, Libin, Ding, Lu, Lin, Shaobin, Wang, Xu, Yang, Xiaoyu, Li, Ping
Publicado 2018

Mutations in FIGLA Associated With Premature Ovarian Insufficiency in a Chinese Population

por Mei, Libin, Huang, Yanru, Wu, Xiaoling, He, Huang, Ye, Ronghui, Ma, Jinxiu, He, XueMei, Shi, Yuhua, Li, Ping
Publicado 2021

Corrigendum: Mutations in FIGLA associated with premature ovarian insufficiency in a Chinese population

por Mei, Libin, Huang, Yanru, Wu, Xiaoling, He, Huang, Ye, Ronghui, Ma, Jinxiu, He, XueMei, Shi, Yuhua, Li, Ping
Publicado 2022

A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy

por Huang, Yanru, Mei, Libin, Wang, Yangdan, Ye, Huiming, Ma, Xiaomin, Zhang, Jian, Cai, Meijiao, Li, Ping, Ge, Yunsheng, Zhou, Yulin
Publicado 2021

Three novel mutations of STK11 gene in Chinese patients with Peutz–Jeghers syndrome

por Tan, Hu, Mei, Libin, Huang, Yanru, Yang, Pu, Li, Haoxian, Peng, Ying, Chen, Chen, Wei, Xianda, Pan, Qian, Liang, Desheng, Wu, Lingqian
Publicado 2016

Turner syndrome with Xp deletions and rare endometrial abnormalities: A case report

por Liang, Lei, Mei, Libin, Shi, Yingying, Huang, Lingling, Su, Zhiying, Zeng, Yu, Gao, Haijie, He, Xuemei, Huang, Hui, Huang, Yanru, Li, Ping, Chen, Jing
Publicado 2021

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia

por Sha, Yanwei, Liu, Wensheng, Huang, Xianjing, Li, Yang, Ji, Zhiyong, Mei, Libin, Lin, Shaobin, Kong, Shuangbo, Lu, Jinhua, Kong, Lingyuan, Zhu, Xingshen, Lu, Zhongxian, Ding, Lu
Publicado 2019