Live birth in a 46‐year‐old woman using microdose GnRH agonist flare‐up protocol combined with GnRH antagonist: a case report

por Zhang, Hong, Liu, Ya‐Qiong, Lu, Guang‐Xiu, Gong, Fei
Publicado 2016

A case of megalencephalic leukoencephalopathy with subcortical cysts type 1 was identified with a novel compound heterozygous alteration (c.135delC; c.423+2dupT) in China

por Dai, Cong‐Ling, He, Wen‐Bin, Du, Juan, Tan, Yue‐Qiu, Lu, Guang‐Xiu, Li, Wen
Publicado 2017

Pregnancy Outcomes of Different Endometrial Preparation in Patients With a History of Cesarean Section

por Gan, Run Xin, Li, Yuan, Song, Juan, Wen, Quan, Lu, Guang Xiu, Lin, Ge, Gong, Fei
Publicado 2022

Telomerase insufficiency induced telomere erosion accumulation in successive generations in dyskeratosis congenita family

por He, Caixia, Jing, Shuang, Dai, Congling, Tu, Chaofeng, Tan, Zhenhua, Du, Juan, Lu, Guang‐Xiu, Lin, Ge, Zeng, Sicong
Publicado 2019

Histological endometrial dating: a reliable tool for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles

por Li, Yuan, Wen, Quan, Hu, Jing, Liao, Jingnan, Fan, Xiangxiu, Chen, Huijun, Zhao, Qi, Lu, Guang-Xiu, Lin, Ge, Gong, Fei
Publicado 2023

The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes

por Xu, Fang, Zhang, Ya-Nan, Cheng, De-Hua, Tan, Ke, Zhong, Chang-Gao, Lu, Guang-Xiu, Lin, Ge, Tan, Yue-Qiu
Publicado 2014

A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome

por Yuan, Shi-Min, Huang, Huan, Tu, Chao-Feng, Du, Juan, Xu, Da-Bao, Lin, Ge, Lu, Guang-Xiu, Tan, Yue-Qiu
Publicado 2018

Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients

por Gu, Yi-Fan, Zhou, Qin-Wei, Zhang, Shuo-Ping, Lu, Chang-Fu, Gong, Fei, Tan, Yue-Qiu, Lu, Guang-Xiu, Lin, Ge
Publicado 2018

Clinical and neonatal outcomes of patients of different ages following transfer of thawed cleavage embryos and blastocysts cultured from thawed cleavage-stage embryos

por Zhou, Qin-Wei, Jing, Shuang, Xu, Li, Guo, Hui, Lu, Chang-Fu, Gong, Fei, Lu, Guang-Xiu, Lin, Ge, Gu, Yi-Fan
Publicado 2018

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

Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency

por He, Wen-Bin, Tan, Yue-Qiu, Hu, Xiao, Li, Wen, Xiong, Bo, Luo, Ke-Li, Gong, Fei, Lu, Guang-Xiu, Lin, Ge, Du, Juan
Publicado 2018

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

Trophectoderm Biopsy Differentially Influences the Level of Serum β-Human Chorionic Gonadotropin With Different Embryonic Trophectoderm Scores in Early Pregnancy From 7847 Single-B...

por Li, Yuan, Wen, Quan, Liao, Jingnan, Ma, Shujuan, Zhang, Shuoping, Gu, Yifan, Tang, Yi, Luo, Keli, Yang, Xiaoyi, Lu, Guang-Xiu, Lin, Ge, Gong, Fei
Publicado 2022

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia

por Wang, Yurong, Liu, Ling, Tan, Chen, Meng, Guiquan, Meng, Lanlan, Nie, Hongchuan, Du, Juan, Lu, Guang-Xiu, Lin, Ge, He, Wen-Bin, Tan, Yue-Qiu
Publicado 2022

Novel FOXL2 mutations cause blepharophimosis‐ptosis‐epicanthus inversus syndrome with premature ovarian insufficiency

por Yang, Xiao‐Wen, He, Wen‐Bin, Gong, Fei, Li, Wen, Li, Xiu‐Rong, Zhong, Chang‐Gao, Lu, Guang‐Xiu, Lin, Ge, Du, Juan, Tan, Yue‐Qiu
Publicado 2018

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

Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations

por Wang, Weili, Tu, Chaofeng, Nie, Hongchuan, Meng, Lanlan, Li, Yong, Yuan, Shimin, Zhang, Qianjun, Du, Juan, Wang, Junpu, Gong, Fei, Fan, Liqing, Lu, Guang-Xiu, Lin, Ge, Tan, Yue-Qiu
Publicado 2019

Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction

por He, Wen-Bin, Xiao, Wen-Juan, Tan, Yue-Qiu, Zhao, Xiao-Meng, Li, Wen, Zhang, Qian-Jun, Zhong, Chang-Gao, Li, Xiu-Rong, Hu, Liang, Lu, Guang-Xiu, Lin, Ge, Du, Juan
Publicado 2018