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CLCN2 chloride channel mutations in familial hyperaldosteronism type II Scholl, Ute I.; Stoelting, Gabriel; Schewe, Julia; Thiel, Anne; Tan, Hua; Nelson-Williams, Carol; Vichot, Alfred A.; Jin, Sheng Chih; Loring, Erin; Untiet, Verena; Yoo, Taekyeong; Choi, Jungmin; Xu, Shengxin; Wu, Aihua; Kirchner, Marieluise; Mertins, Philipp; Rump, Lars C.; Onder, Ali Mirza; Gamble, Cory; McKenney, Daniel; Lash, Robert W.; Jones, Deborah P.; Chune, Gary; Gagliardi, Priscila; Choi, Murim; Gordon, Richard; Stowasser, Michael; Fahlke, Christoph; Lifton, Richard P. 分享 收藏
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Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome) Glover, Mark; Ware, James S.; Henry, Amanda; Wolley, Martin; Walsh, Roddy; Wain, Louise V.; Xu, Shengxin; Van't Hoff, William G.; Tobin, Martin D.; Hall, Ian P.; Cook, Stuart; Gordon, Richard D.; Stowasser, Michael; O'Shaughnessy, Kevin M. 分享 收藏
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A single nucleotide polymorphism of MHC region is associated with subphenotypes of Psoriasis in Chinese population Zheng, Hou-Feng; Zhang, Chi; Sun, Liang-Dan; Ni, Cheng; Zuo, Xian-Bo; Zhang, Zheng; Lu, Wen-Sheng; Xu, Sheng-Xin; Han, Jian-Wen; Cheng, Hui; Zhu, Kun-Ju; Cheng, Yi-Lin; Yang, Sen; Zhang, Feng-Yu; Zhang, Xue-Jun 分享 收藏
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC 白癜风的全基因组关联研究确定了6q27和MHC的易感基因位点 Quan, Cheng; Ren, Yun-Qing; Xiang, Lei-Hong; Sun, Liang-Dan; Xu, Ai-E; Gao, Xing-Hua; Chen, Hong-Duo; Pu, Xiong-Ming; Wu, Ri-Na; Liang, Chao-Zhao; Li, Jia-Bin; Gao, Tian-Wen; Zhang, Jian-Zhong; Wang, Xiu-Li; Wang, Jun; Yang, Rong-Ya; Liang, Ling; Yu, Jian-Bin; Zuo, Xian-Bo; Zhang, Sheng-Quan; Zhang, Shu-Mei; Chen, Gang; Zheng, Xiao-Dong; Li, Pan; Zhu, Jun; Li, Yong-Wei; Wei, Xiao-Dong; Hong, Wei-Song; Ye, Ying; Zhang, Yong; Wu, Wei-Su; Cheng, Hui; Dong, Pu-Ling; Hu, Da-Yan; Li, Yang; Li, Min; Zhang, Xin; Tang, Hua-Yang; Tang, Xian-Fa; Xu, Sheng-Xin; He, Su-Min; Lv, Yong-Mei; Shen, Min; Jiang, Hong-Quan; Wang, Ying; Li, Kai; Kang, Xiao-Jing; Liu, Yu-Qin; Sun, Li; Liu, Zhi-Fang; Xie, Shao-Qiong; Zhu, Cheng-Yao; Xu, Qiang; Gao, Jin-Ping; Hu, Wen-Long; Ni, Cheng; Pan, Ting-Meng; Li, Yun; Yao, Sha; He, Cai-Feng; Liu, Yang-Sheng; Yu, Ze-Ying; Yin, Xian-Yong; Zhang, Feng-Yu; Yang, Sen; Zhou, Youwen; Zhang, Xue-Jun 分享 收藏
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A novel U2HR non-synonymous mutation in a Chinese patient with Marie Unna Hereditary Hypotrichosis Cai, Li-Qiong; Wang, Pei-Guang; Gao, Min; Lu, Wen-Sheng; Xu, Sheng-Xin; Fang, Qiao-Yun; Zhou, Wen-Ming; Lin, Da; Du, Wen-Hui; Zhang, Shu-Mei; Yang, Sen; Zhang, Xue-Jun 分享 收藏
Genetic Variation of Promoter Sequence Modulates XBP1 Expression and Genetic Risk for Vitiligo Ren, Yunqing; Yang, Sen; Xu, Shengxin; Gao, Min; Huang, Wei; Gao, Tianwen; Fang, Qiaoyun; Quan, Cheng; Zhang, Chi; Sun, Liangdan; Liang, Yanhua; Han, Jianwen; Wang, Zhimin; Zhang, Fengyu; Zhou, Youwen; Liu, Jianjun; Zhang, Xuejun 分享 收藏
Follow-up analysis of 180 Chinese Han families: identification of a novel locus for psoriasis at 2p22.3-11.2 Sun, L. D.; Yang, S.; Liu, J. J.; Ren, Y. Q.; Fan, X.; Xu, S. X.; Zhou, L.; Yang, C. J.; Xiao, F. L.; Gao, M.; Cui, Y.; Du, W. H.; Huang, W.; Zhang, X. J. 分享 收藏
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