Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic a...

by Zheng, Bixia, Hu, Guorui, Yu, Jin, Liu, Zhifeng
Published 2014

A novel Bruton’s tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia

by Zheng, Bixia, Zhang, Yayuan, Jin, Yu, Yu, Haiguo
Published 2014

Association of Base Excision Repair Gene Polymorphisms with ESRD Risk in a Chinese Population

by Cai, Zhenming, Chen, Huimei, Tao, Jing, Guo, Wenwen, Liu, Xiufang, Zheng, Bixia, Sun, Wei, Wang, Yaping
Published 2012

The Polymorphic AluYb8 Insertion in the MUTYH Gene is Associated with Reduced Type 1 Protein Expression and Reduced Mitochondrial DNA Content

by Guo, Wenwen, Zheng, Bixia, Cai, Zhenming, Xu, Lizhi, Guo, Dong, Cao, Lili, Wang, Yaping
Published 2013

Diagnosis of ABCB11 gene mutations in children with intrahepatic cholestasis using high resolution melting analysis and direct sequencing

by HU, GUORUI, HE, PING, LIU, ZHIFENG, CHEN, QIAN, ZHENG, BIXIA, ZHANG, QIHUA
Published 2014