A novel loss-of-function variant in PNLDC1 inducing oligo-astheno-teratozoospermia and male infertility

por Zhao, Si-Yi, Meng, Lan-Lan, Du, Zhao-Li, Tan, Yue-Qiu, He, Wen-Bin, Wang, Xiong
Publicado 2023

In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency

por Xiao, Wen-Juan, He, Wen-Bin, Zhang, Ya-Xin, Meng, Lan-Lan, Lu, Guang-Xiu, Lin, Ge, Tan, Yue-Qiu, Du, Juan
Publicado 2019

Homozygous variants in SYCP2L cause premature ovarian insufficiency

por He, Wen-Bin, Tan, Chen, Zhang, Ya-Xin, Meng, Lan-Lan, Gong, Fei, Lu, Guang-Xiu, Lin, Ge, Du, Juan, Tan, Yue-Qiu
Publicado 2021

Phenotypic and molecular characteristics of androgen insensitivity syndrome patients

por Yuan, Shi-Min, Zhang, Ya-Nan, Du, Juan, Li, Wen, Tu, Chao-Feng, Meng, Lan-Lan, Lin, Ge, Lu, Guang-Xiu, Tan, Yue-Qiu
Publicado 2018

Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency

por Zhang, Ya‐Xin, He, Wen‐Bin, Xiao, Wen‐Juan, Meng, Lan‐Lan, Tan, Chen, Du, Juan, Lu, Guang‐Xiu, Lin, Ge, Tan, Yue‐Qiu
Publicado 2020

A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans

por Li, Yong, Wang, Wei-Li, Tu, Chao-Feng, Meng, Lan-Lan, Hu, Tong-Yao, Du, Juan, Lin, Ge, Nie, Hong-Chuan, Tan, Yue-Qiu
Publicado 2020

Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans

por Li, Dong-Yan, Yang, Xiao-Xuan, Tu, Chao-Feng, Wang, Wei-Li, Meng, Lan-Lan, Lu, Guang-Xiu, Tan, Yue-Qiu, Zhang, Qian-Jun, Du, Juan
Publicado 2021