P. Li

A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole‐exome sequencing

X. Xu, Ping Li, H. Ji, 2018, Clinical genetics.

Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development.

C. Chen, X. Zhang, S. Zhao, 2018, Human Reproduction.

Headless spermatozoa in infertile men

X. Wang, Y. Sha, Zhiyong Ji, 2017, Andrologia.

DNAH6 is a novel candidate gene associated with sperm head anomaly

X. Xu, C. Yin, C. Wang, 2018, Andrologia.

TSGA10 is a novel candidate gene associated with acephalic spermatozoa

X. Xu, X. Wang, Q. Zhang, 2018, Clinical genetics.