A novel mutation in EYA1 in a Chinese family with Branchio-oto-renal syndrome

por Wang, Yan-gong, Sun, Shu-ping, Qiu, Yi-ling, Xing, Qing-he, Lu, Wei
Publicado en BMC Med Genet (2018)

A Gene Locus Responsible for Dyschromatosis Symmetrica Hereditaria (DSH) Maps to Chromosome 6q24.2-q25.2

por Xing, Qing-he, Wang, Ming-tai, Chen, Xiang-dong, Feng, Guo-yin, Ji, Hong-yun, Yang, Jian-dong, Gao, Jian-jun, Qin, Wei, Qian, Xue-qing, Wu, Sheng-nan, He, Lin
Publicado 2003

Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

por Qiu, Yi‐Ling, Gong, Jing‐Yu, Feng, Jia‐Yan, Wang, Ren‐Xue, Han, Jun, Liu, Teng, Lu, Yi, Li, Li‐Ting, Zhang, Mei‐Hong, Sheps, Jonathan A., Wang, Neng‐Li, Yan, Yan‐Yan, Li, Jia‐Qi, Chen, Lian, Borchers, Christoph H., Sipos, Bence, Knisely, A.S., Ling, Victor, Xing, Qing‐He, Wang, Jian‐She
Publicado en Hepatology (2017)