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SaveShare Save Share Save Share Save Whole-genome sequencing analysis in fetal structural anomalies: novel phenotype-genotype discoveries
Qi, Q.; Jiang, Y.; Zhou, X.; Lu, Y.; Xiao, R.; Bai, J.; Lou, H.; Sun, W.; Lian, Y.; Hao, N.; Li, M.; Chang, J. Share Save Share Save Share Save Optimal Value for Serum Anti-PLA2R Antibody in Primary Membranous Nephropathy: A Multicenter Observational StudyChen, Juan; Jia, Xiaoyan; Wei, Xin; Li, Jiao; Liu, Yipeng; Lian, Ying; Cui, Zhao; Zhao, Minghui; Luan, Sen; Zhang, Minghui; Mi, Jie; Wang, Dongyan; Xu, Dongmei Share Save Share Save Share Save Prophylactic administration of fingolimod (FTY720) ameliorated experimental autoimmune myasthenia gravis by reducing the number of dendritic cells, follicular T helper cells and antibody-secreting cellsLiu, Ying; Yang, Chun-Lin; Yang, Bing; Du, Tong; Li, Xiao-Li; Zhang, Peng; Ge, Meng-Ru; Lian, Ying; Li, Heng; Liu, Yu-Dong; Duan, Rui-Sheng Share Save Share Save Share Save Very-low-dose decitabine treatment for patients with intermediate- or high-risk myelodysplastic syndrome: a retrospective analysis of thirteen casesZhang, Kaiji; Lian, Ying; Guan, Xiaohong; Hu, Qian; Lei, Lihua; Tao, Li; He, Dong; Lin, Juan; Hou, Zheng; Ren, Lirong; Liu, Xiaoxiao; Ren, Qian; Pan, Lin; Fei, Xiaoli; Xiong, Mei; Wen, Shunzhu; Cao, Jinzhu Share Save Meta-Analysis of the Diagnostic Efficiency of THSD7A-AB for the Diagnosis of Idiopathic Membranous NephropathyLiu, Yipeng; Zheng, Shanshan; Ma, Chaoqun; Lian, Ying; Zheng, Xiaoli; Guan, Peizhong; Wang, Baobao; Gong, Xiaojie; Gao, Feng; Liang, Liming; Xu, Dongmei Share Save A novel pathogenic mutation in FBN2 associated with congenital contractural arachnodactyly for preimplantation genetic diagnosisLi, Jiaxin; Wang, Yuqian; Zhu, Xiaohui; Nie, Yanli; Kuo, Ying; Guan, Shuo; Huang, Jin; Lian, Ying; Zhao, Yangyu; Li, Rong; Wei, Yuan; Qiao, Jie; Yan, Liying Share Save Share Save Share Save Share Save Share Save 
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