Novel homozygous protein‐truncating mutation of BBS9 identified in a Chinese consanguineous family with Bardet–Biedl syndrome

por Tang, Hai‐Yan, Xie, Fen, Dai, Ru‐Chun, Shi, Xiao‐Liu
Publicado 2021

Effects of aspirin and enoxaparin in a rat model of liver fibrosis

por Li, Chen-Jie, Yang, Zhi-Hui, Shi, Xiao-Liu, Liu, De-Liang
Publicado 2017

Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome

por Wu, Bo-Da, Wang, Yong-Jun, Fan, Liang-Liang, Huang, Hui, Zhou, Peng, Yang, Mei, Shi, Xiao-Liu
Publicado 2020