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

Por Zheng, Bixia, Zhang, Yayuan, Jin, Yu, Yu, Haiguo
Publicado no BMC Pediatr (2014)

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...

Por Zheng, Bixia, Hu, Guorui, Yu, Jin, Liu, Zhifeng
Publicado no BMC Pediatr (2014)

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

Por HU, GUORUI, HE, PING, LIU, ZHIFENG, CHEN, QIAN, ZHENG, BIXIA, ZHANG, QIHUA
Publicado em 2014

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

Por Guo, Wenwen, Zheng, Bixia, Cai, Zhenming, Xu, Lizhi, Guo, Dong, Cao, Lili, Wang, Yaping
Publicado em 2013

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

Por Cai, Zhenming, Chen, Huimei, Tao, Jing, Guo, Wenwen, Liu, Xiufang, Zheng, Bixia, Sun, Wei, Wang, Yaping
Publicado em 2012