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

by Ya-Qi Tan, Yue-Qiu Tan, De-Hua Cheng
Published 2020-05-01

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

by Wei-Li Wang, Chao-Feng Tu, Yue-Qiu Tan
Published 2020-01-01

Effect of thyroid autoimmunity per se on assisted reproduction treatment outcomes: A meta-analysis

by Hui He, Shuang Jing, Fei Gong, Yue Qiu Tan, Guang Xiu Lu, Ge Lin
Published 2016-04-01

In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency

by Wen-Juan Xiao, Wen-Bin He, Wen-Bin He, Wen-Bin He, Ya-Xin Zhang, Lan-Lan Meng, Lan-Lan Meng, Guang-Xiu Lu, Guang-Xiu Lu, Guang-Xiu Lu, Ge Lin, Ge Lin, Ge Lin, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan, Juan Du, Juan Du, Juan Du
Published 2019-11-01

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

by Aixiang Luo, Dehua Cheng, Shimin Yuan, Haiyu Li, Juan Du, Yang Zhang, Chuanchun Yang, Ge Lin, Wenyong Zhang, Yue-Qiu Tan
Published 2018-04-01

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

by Shi-Min Yuan, Huan Huang, Chao-Feng Tu, Juan Du, Da-Bao Xu, Ge Lin, Guang-Xiu Lu, Yue-Qiu Tan
Published 2018-01-01

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

by Yi-Fan Gu, Qin-Wei Zhou, Shuo-Ping Zhang, Chang-Fu Lu, Fei Gong, Yue-Qiu Tan, Guang-Xiu Lu, Ge Lin
Published 2018-01-01

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

by Ya‐Xin Zhang, Wen‐Bin He, Wen‐Juan Xiao, Lan‐Lan Meng, Chen Tan, Juan Du, Guang‐Xiu Lu, Ge Lin, Yue‐Qiu Tan
Published 2020-04-01

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

by Wen-Bin He, Yue-Qiu Tan, Xiao Hu, Wen Li, Bo Xiong, Ke-Li Luo, Fei Gong, Guang-Xiu Lu, Ge Lin, Juan Du
Published 2018-01-01

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

by Yong Li, Wei-Li Wang, Chao-Feng Tu, Lan-Lan Meng, Tong-Yao Hu, Juan Du, Ge Lin, Hong-Chuan Nie, Yue-Qiu Tan
Published 2021-01-01

Etiological Analysis of Neurodevelopmental Disabilities: Single-Center Eight-Year Clinical Experience in South China

by Li Guo, Bing-Xiao Li, Mei Deng, Fang Wen, Jian-Hui Jiang, Yue-Qiu Tan, Yuan-Zong Song, Zhen-Huan Liu, Chun-Hua Zhang, Keiko Kobayashi, Zi-Neng Wang
Published 2011-01-01

Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature

by Haiyu Li, Juan Du, Wen Li, Dehua Cheng, Wenbin He, Duo Yi, Bo Xiong, Shimin Yuan, Chaofeng Tu, Lanlan Meng, Aixiang Luo, Ge Lin, Guangxiu Lu, Yue-Qiu Tan
Published 2018-02-01

Improving native human sperm freezing protection by using a modified vitrification method

by Dai Zhou, Xing-Ming Wang, Rui-Xue Li, Yi-Ze Wang, Yuan-Chi Chao, Zhi-Zhong Liu, Zeng-Hui Huang, Hong-Chuan Nie, Wen-Bing Zhu, Yue-Qiu Tan, Li-Qing Fan
Published 2021-01-01

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

by Wen-Bin He, Wen-Juan Xiao, Yue-Qiu Tan, Xiao-Meng Zhao, Wen Li, Qian-Jun Zhang, Chang-Gao Zhong, Xiu-Rong Li, Liang Hu, Guang-Xiu Lu, Ge Lin, Juan Du
Published 2018-10-01

Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism

by Xiao Hu, Wen‐Bin He, Shuo‐Ping Zhang, Ke‐Li Luo, Fei Gong, Jing Dai, Yi Zhang, Zhen‐Xing Wan, Wen Li, Shi‐Min Yuan, Yue‐Qiu Tan, Guang‐Xiu Lu, Ge Lin, Juan Du
Published 2021-05-01