Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype von Sha, Yanwei, Wei, Xiaoli, Ding, Lu, Ji, Zhiyong, Mei, Libin, Huang, Xianjing, Su, Zhiying, Wang, Wenrong, Zhang, Xuequan, Lin, Shaobin

Volltext

DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella von Li, Yang, Sha, Yanwei, Wang, Xiong, Ding, Lu, Liu, Wensheng, Ji, Zhiyong, Mei, Libin, Huang, Xianjing, Lin, Shaobin, Kong, Shuangbo, Lu, Jinhua, Qin, Weibing, Zhang, Xinzhong, Zhuang, Jianmin, Tang, Yunge, Lu, Zhongxian

Volltext

Day 2 versus day 3 embryo transfer in patients with in vitro fertilization and only one zygote with two pronuclei von Ye, Yaping, Huang, Hui, Wang, Longmei, Ding, Lu, Mei, Libin, Li, Ping

Volltext

DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella von Sha, Yanwei, Wei, Xiaoli, Ding, Lu, Mei, Libin, Huang, Xianjing, Lin, Shaobin, Su, Zhiying, Kong, Lingyuan, Zhang, Yi, Ji, Zhiyong

Volltext

Preparation and kinetic study of organic amine‐loaded ion‐exchange resin as CO2 adsorbents von Liu, Xinmin, Qiu, Xuexia, Sun, Xin, Mei, Libin, Wang, Lingyun, Guo, Qingjie

Volltext

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review von Sha, Yanwei, Zheng, Liangkai, Ji, Zhiyong, Mei, Libin, Ding, Lu, Lin, Shaobin, Wang, Xu, Yang, Xiaoyu, Li, Ping

Volltext

A familial analysis of two brothers with azoospermia caused by maternal 46,Y, t(X; 1) (q28; q21) chromosomal abnormality von Li, Youzhu, Sha, Yanwei, Wei, Zijie, Liu, Wensheng, Mei, Libin, hong, Yun, Jiang, Lizhi, Ge, Yunsheng, Xie, Yuanzhi

Volltext

Preimplantation genetic testing for Cockayne syndrome with a novel ERCC6 variant in a Chinese family von He, Xuemei, Zhang, Yiyuan, Huang, Xianjing, Qiu, Pingping, Ji, Hong, Ding, Lu, Shi, Yingying, Huang, Yanru, Li, Ping, Mei, Libin

Volltext

Preimplantation Genetic Testing Inhibits the Transmission of Pathogenic Variants Associated With Cerebral White Matter Disease von Huang, Xianjing, Qiu, Pingping, Ji, Hong, Shi, Yingying, Zhang, Ling, Wang, Longmei, Mei, Libin, Li, Ping

Volltext

A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy von Huang, Yanru, Mei, Libin, Wang, Yangdan, Ye, Huiming, Ma, Xiaomin, Zhang, Jian, Cai, Meijiao, Li, Ping, Ge, Yunsheng, Zhou, Yulin

Volltext

Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome von Tan, Hu, Mei, Libin, Huang, Yanru, Yang, Pu, Li, Haoxian, Peng, Ying, Chen, Chen, Wei, Xianda, Pan, Qian, Liang, Desheng, Wu, Lingqian

Volltext

Mutations in FIGLA Associated With Premature Ovarian Insufficiency in a Chinese Population von Mei, Libin, Huang, Yanru, Wu, Xiaoling, He, Huang, Ye, Ronghui, Ma, Jinxiu, He, XueMei, Shi, Yuhua, Li, Ping

Volltext

Corrigendum: Mutations in FIGLA associated with premature ovarian insufficiency in a Chinese population von Mei, Libin, Huang, Yanru, Wu, Xiaoling, He, Huang, Ye, Ronghui, Ma, Jinxiu, He, XueMei, Shi, Yuhua, Li, Ping

Volltext

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia von 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

Volltext

DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population von Sha, Yanwei, M.D, Yang, Xiaoyu, M.D, Mei, Libing, M.D, Ji, Zhiyong, M.D, Wang, Xu, M.D, Ding, Lu, M.D, Li, Ping, M.D, Yang, Shenmin, M.D

Volltext

Two novel biallelic mutations in PSMC3IP in a patient affected by premature ovarian insufficiency von Mei, Libin, Huang, Lingling, Huang, Yanru, Wu, Xiaoling, He, Huang, He, Xuemei, Su, Zhiying, Li, Ping

Volltext

Turner syndrome with Xp deletions and rare endometrial abnormalities: A case report von Liang, Lei, Mei, Libin, Shi, Yingying, Huang, Lingling, Su, Zhiying, Zeng, Yu, Gao, Haijie, He, Xuemei, Huang, Hui, Huang, Yanru, Li, Ping, Chen, Jing

Volltext

Two novel NIPBL gene mutations in Chinese patients with Cornelia de Lange syndrome von Mei, Libin, Liang, Desheng, Huang, Yanru, Pan, Qian, Wu, Lingqian

Volltext

Day 2 versus day 3 embryo transfer in patients with fertilization and only one zygote with two pronuclei von Yaping Ye, Hui Huang, Longmei Wang, Lu Ding, Libin Mei, Ping Li

Volltext

Two novel biallelic mutations in PSMC31P in a patient affected by premature ovarian insufficiency von Mei, Libin, Huang, Lingling, Huang, Yanru, Wu, Xiaoling, He, Huang, He, Xuemei, Su, Zhiying, Li, Ping

Volltext