Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome

por Yuan, Zhuang-Zhuang, Xie, Xiao-Hui, Gu, Heng, Zhang, Wei-Zhi, Hu, Yi-Qiao, Yang, Yi-Feng, Tan, Zhi-Ping
Publicado 2021

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 2014

Is elevated SUA associated with a worse outcome in young Chinese patients with acute cerebral ischemic stroke?

por Zhang, Bin, Gao, Cong, Yang, Ning, Zhang, WeiZhi, Song, XingWang, Yin, JianRui, Pu, ShuXiang, Yi, YongHong, Gao, QingChun
Publicado 2010

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 2014