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

par Wang, Yan-gong, Sun, Shu-ping, Qiu, Yi-ling, Xing, Qing-he, Lu, Wei
Publié dans BMC Med Genet (2018)

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

par 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
Publié 2003

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

par 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
Publié dans Hepatology (2017)