Reversible insulator-metal transition of LaAlO(3)/SrTiO(3) interface for nonvolatile memory

Por Lu, Hong-Liang, Liao, Zhi-Min, Zhang, Liang, Yuan, Wen-Tao, Wang, Yong, Ma, Xiu-Mei, Yu, Da-Peng
Publicado em 2013

A Novel Linkage to Generalized Vitiligo on 4q13-q21 Identified in a Genomewide Linkage Analysis of Chinese Families

Por Chen, Jian-Jun, Huang, Wei, Gui, Jin-Ping, Yang, Sen, Zhou, Fu-Sheng, Xiong, Quan-Geng, Wu, Hong-Bo, Cui, Yong, Gao, Min, Li, Wei, Li, Jin-Xian, Yan, Kai-Lin, Yuan, Wen-Tao, Xu, Shi-Jie, Liu, Jian-Jun, Zhang, Xue-Jun
Publicado em 2005

A Nonsense Mutation in DHTKD1 Causes Charcot-Marie-Tooth Disease Type 2 in a Large Chinese Pedigree

Por Xu, Wang-yang, Gu, Ming-min, Sun, Lian-hua, Guo, Wen-ting, Zhu, Hou-bao, Ma, Jian-fang, Yuan, Wen-tao, Kuang, Ying, Ji, Bao-jun, Wu, Xiao-lin, Chen, Yan, Zhang, Hong-xin, Sun, Fu-ting, Huang, Wei, Huang, Lei, Chen, Sheng-di, Wang, Zhu-gang
Publicado em 2012

Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene

Por Wu, Xiao-lin, Gu, Ming-min, Huang, Lei, Liu, Xue-song, Zhang, Hong-xin, Ding, Xiao-yi, Xu, Jian-qiang, Cui, Bin, Wang, Long, Lu, Shun-yuan, Chen, Xiao-yi, Zhang, Hai-guo, Huang, Wei, Yuan, Wen-tao, Yang, Jiang-ming, Gu, Qun, Fei, Jian, Chen, Zhu, Yuan, Zhi-min, Wang, Zhu-gang
Publicado em 2009