Advances in Identification of Susceptibility Gene Defects of Hereditary Colorectal Cancer

por Liu, Qiang, Tan, Yue-Qiu
Publicado 2019

Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies

por Tan, Ya-Qi, Tan, Yue-Qiu, Cheng, De-Hua
Publicado 2020

Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new?

por Wang, Wei-Li, Tu, Chao-Feng, Tan, Yue-Qiu
Publicado 2019

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

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

Risk Factors Affecting Alternate Segregation in Blastocysts From Preimplantation Genetic Testing Cycles of Autosomal Reciprocal Translocations

por Xie, Pingyuan, Hu, Liang, Peng, Yangqin, Tan, Yue-qiu, Luo, Keli, Gong, Fei, Lu, Guangxiu, Lin, Ge
Publicado 2022

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

Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings

por Luo, Aixiang, Cheng, Dehua, Yuan, Shimin, Li, Haiyu, Du, Juan, Zhang, Yang, Yang, Chuanchun, Lin, Ge, Zhang, Wenyong, Tan, Yue-Qiu
Publicado 2018

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

DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice

por Zhou, Shushu, Yuan, Shimin, Zhang, Jintao, Meng, Lanlan, Zhang, Xin, Liu, Siyu, Lu, Guangxiu, Lin, Ge, Liu, Mingxi, Tan, Yue-Qiu
Publicado 2023

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

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

Clinical outcomes following preimplantation genetic testing and microdissecting junction region in couples with balanced chromosome rearrangement

por Cheng, Dehua, Hu, Liang, Gong, Fei, Yuan, Shimin, Luo, Keli, Wu, Xianhong, Xie, Pingyuan, Lu, Changfu, Lu, Guangxiu, Tan, Yue-Qiu, Lin, Ge
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

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

Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella

por Tu, Chaofeng, Nie, Hongchuan, Meng, Lanlan, Yuan, Shimin, He, Wenbin, Luo, Aixiang, Li, Haiyu, Li, Wen, Du, Juan, Lu, Guangxiu, Lin, Ge, Tan, Yue-Qiu
Publicado 2019

A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance

por Bai, Rui‐Qi, He, Wen‐Bin, Peng, Qian, Shen, Su‐Hui, Yu, Qian‐Qian, Du, Juan, Tan, Yue‐Qiu, Wang, Yue‐Hong, Liu, Bin‐Jie
Publicado 2022