Highly precise breakpoint detection of chromosome balanced translocation in chronic myelogenous leukaemia: Case series

por Yang, Chuanchun, Cui, Xiaoli, Xu, Lei, Zhang, Qian, Tang, Shanmei, Zhang, Mengmeng, Xie, Ni
Publicado 2022

Analysis of complex chromosomal rearrangements using a combination of current molecular cytogenetic techniques

por He, Ping, Wei, Xiaoni, Xu, Yuchan, Huang, Jun, Tang, Ning, Yan, Tizhen, Yang, Chuanchun, Lu, Kangmo
Publicado 2022

Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional Techniques

por Pan, Qiong, Hu, Hao, Han, Liangrong, Jing, Xin, Liu, Hailiang, Yang, Chuanchun, Zhang, Fengting, Hu, Yue, Yue, Hongni, Ning, Ying
Publicado 2016

Successful birth after preimplantation genetic testing for a couple with two different reciprocal translocations and review of the literature

por Liu, Dun, Chen, Chuangqi, Zhang, Xiqian, Dong, Mei, He, Tianwen, Dong, Yunqiao, Lu, Jian, Yu, Lihua, Yang, Chuanchun, Liu, Fenghua
Publicado 2021

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

Breakpoints and deleted genes identification of ring chromosome 18 in a Chinese girl by whole-genome low-coverage sequencing: a case report study

por Yao, Hui, Yang, Chuanchun, Huang, Xiaoli, Yang, Luhong, Zhao, Wei, Yin, Dan, Qin, Yuan, Mu, Feng, Liu, Lin, Tian, Ping, Liu, Zhisheng, Yang, Yun
Publicado 2016

Successful pregnancy after prenatal diagnosis by NGS for a carrier of complex chromosome rearrangements

por Ou, Jian, Yang, Chuanchun, Cui, Xiaoli, Chen, Chuan, Ye, Suyan, Zhang, Cai, Wang, Kai, Chen, Jianguo, Zhang, Qin, Qian, Chunfeng, Fang, Guangguang, Zhang, Wenyong
Publicado 2020

A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR gene

por Wang, Liping, Lin, Weisheng, Li, Xiaohong, Zhang, Lijuan, Wang, Kai, Cui, Xiaoli, Tang, Shanmei, Fang, Guangguang, Tan, Yan, Wang, Xuelai, Chen, Chuan, Yang, Chuanchun, Tang, Huiru
Publicado 2021

A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case report

por Fu, Dalin, Lin, Weisheng, Lu, Fen, Du, Senjie, Zhu, Min, Zhao, Xiaoke, Tang, Jian, Chen, Chuan, Chui, Xiaoli, Tang, Shanmei, Wang, Kai, Yang, Chuanchun, Han, Bei
Publicado 2021

Screening of triploid with low-coverage whole-genome sequencing by a single-nucleotide polymorphism-based test in miscarriage tissue

por Geng, Qian, Cui, Xiaoli, Zhang, Yaqi, Zhang, Lijuan, Zhang, Cai, Wang, Kai, Chen, Jianguo, Zhu, Qingyan, Xie, Jiansheng, Xu, Zhiyong, Liu, Yang, Zhang, MengMeng, Ding, Lijie, Zhang, Wenyong, Yang, Chuanchun
Publicado 2019

Systematic analysis of microbiota in pregnant Chinese women and its association with miscarriage

por Guang, Yu, Shen, Xiao, Tan, Yan, Tang, Shanmei, Chen, Jing, Zhang, Longhui, Wang, Baohong, Ye, Suyan, Chen, Xiaomei, Yang, Chuanchun, Chen, Chuan, Li, Guanglei, Chen, Jianguo, Cui, Xiaoli, Lin, Weisheng, Wang, Xuelai, Fang, Guangguang
Publicado 2022