A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal...

Por Liu, Ji-jia, Fan, Liang-liang, Chen, Jin-lan, Tan, Zhi-ping, Yang, Yi-feng
Publicado em 2014

Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11

Por Chen, Jin-Lan, Zhu, Xin, Zhao, Tian-Li, Wang, Jian, Yang, Yi-Feng, Tan, Zhi-Ping
Publicado em 2014

Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death

Por Tan, Zhi-Ping, Xie, Li, Deng, Yao, Chen, Jin-Lan, Zhang, Wei-Zhi, Wang, Jian, Yang, Jin-Fu, Yang, Yi-Feng
Publicado no Sci Rep (2014)

Rare De Novo Copy Number Variants in Patients with Congenital Pulmonary Atresia

Por Xie, Li, Chen, Jin-Lan, Zhang, Wei-Zhi, Wang, Shou-Zheng, Zhao, Tian-Li, Huang, Can, Wang, Jian, Yang, Jin-Fu, Yang, Yi-Feng, Tan, Zhi-Ping
Publicado em 2014