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

gan Pan, Qiong, Hu, Hao, Han, Liangrong, Jing, Xin, Liu, Hailiang, Yang, Chuanchun, Zhang, Fengting, Hu, Yue, Yue, Hongni, Ning, Ying
Cyhoeddwyd yn PLoS One (2016)

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

gan Liu, Dun, Chen, Chuangqi, Zhang, Xiqian, Dong, Mei, He, Tianwen, Dong, Yunqiao, Lu, Jian, Yu, Lihua, Yang, Chuanchun, Liu, Fenghua
Cyhoeddwyd yn Reprod Biol Endocrinol (2021)

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

gan Luo, Aixiang, Cheng, Dehua, Yuan, Shimin, Li, Haiyu, Du, Juan, Zhang, Yang, Yang, Chuanchun, Lin, Ge, Zhang, Wenyong, Tan, Yue-Qiu
Cyhoeddwyd yn Mol Cytogenet (2018)

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

gan Yao, Hui, Yang, Chuanchun, Huang, Xiaoli, Yang, Luhong, Zhao, Wei, Yin, Dan, Qin, Yuan, Mu, Feng, Liu, Lin, Tian, Ping, Liu, Zhisheng, Yang, Yun
Cyhoeddwyd yn BMC Med Genet (2016)

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

gan Ou, Jian, Yang, Chuanchun, Cui, Xiaoli, Chen, Chuan, Ye, Suyan, Zhang, Cai, Wang, Kai, Chen, Jianguo, Zhang, Qin, Qian, Chunfeng, Fang, Guangguang, Zhang, Wenyong
Cyhoeddwyd yn Reprod Biol Endocrinol (2020)

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

gan 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
Cyhoeddwyd yn Medicine (Baltimore) (2021)

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

gan 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
Cyhoeddwyd yn BMC Pediatr (2021)

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

gan 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
Cyhoeddwyd yn J Assist Reprod Genet (2019)