Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and EGR2[original query] |
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Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
Nature genetics 2014 Sep 46 (9): 1007-11. Hou Shengping, Du Liping, Lei Bo, Pang Chi Pui, Zhang Meifen, Zhuang Wenjuan, Zhang Minglian, Huang Lulin, Gong Bo, Wang Meilin, Zhang Qi, Hu Ke, Zhou Qingyun, Qi Jian, Wang Chaokui, Tian Yuan, Ye Zi, Liang Liang, Yu Hongsong, Li Hong, Zhou Yan, Cao Qingfeng, Liu Yunjia, Bai Lin, Liao Dan, Kijlstra Aize, Xu Jianfeng, Yang Zhenglin, Yang Peize |
Investigation of the association of Vogt-Koyanagi-Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai. The British journal of ophthalmology 2015 Dec . Cao Shuang, Chee Soon Phaik, Yu Hyeong Gon, Sukavatcharin Somsiri, Wu Lili, Kijlstra Aize, Hou Shengping, Yang Peize |
Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing. PloS one 2017 12 (10): e0185602. Lee Jee-Soo, Seo Heewon, Im Kyongok, Park Si Nae, Kim Sung-Min, Lee Eun Kyoung, Kim Jung-Ah, Lee Joon-Hee, Kwon Sunghoon, Kim Miyoung, Koh Insong, Hwang Seungwoo, Park Heung-Woo, Kang Hye-Ryun, Park Kyoung Soo, Kim Ju Han, Lee Dong So |
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