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

per Wang, Yan-gong, Sun, Shu-ping, Qiu, Yi-ling, Xing, Qing-he, Lu, Wei
Publicat a BMC Med Genet (2018)

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

per 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
Publicat 2003

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

per 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
Publicat a Hepatology (2017)