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

von Wang, Yan-gong, Sun, Shu-ping, Qiu, Yi-ling, Xing, Qing-he, Lu, Wei
Veröffentlicht in BMC Med Genet (2018)

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

von 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
Veröffentlicht 2003

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

von 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
Veröffentlicht in Hepatology (2017)