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Association of novel rare coding variants with juvenile idiopathic arthritis.
Meng X, Hou X, Wang P, Glessner JT, Qu HQ, March ME, Zhang S, Qi X, Zhu C, Nguyen K, Gao X, Li X, Liu Y, Zhou W, Zhang S, Li J, Sun Y, Yang J, Sleiman PMA, Xia Q, Hakonarson H, Li J. Meng X, et al. Among authors: li j, li x. Ann Rheum Dis. 2021 May;80(5):626-631. doi: 10.1136/annrheumdis-2020-218359. Epub 2021 Jan 6. Ann Rheum Dis. 2021. PMID: 33408077
Altered Urinary Amino Acids in Children With Autism Spectrum Disorders.
Liu A, Zhou W, Qu L, He F, Wang H, Wang Y, Cai C, Li X, Zhou W, Wang M. Liu A, et al. Among authors: li x. Front Cell Neurosci. 2019 Jan 25;13:7. doi: 10.3389/fncel.2019.00007. eCollection 2019. Front Cell Neurosci. 2019. PMID: 30733669 Free PMC article.
Gene4HL: An Integrated Genetic Database for Hearing Loss.
Huang S, Zhao G, Wu J, Li K, Wang Q, Fu Y, Zhang H, Bi Q, Li X, Wang W, Guo C, Zhang D, Wu L, Li X, Xu H, Han M, Wang X, Lei C, Qiu X, Li Y, Li J, Dai P, Yuan Y. Huang S, et al. Among authors: li y, li j, li x, li k. Front Genet. 2021 Oct 18;12:773009. doi: 10.3389/fgene.2021.773009. eCollection 2021. Front Genet. 2021. PMID: 34733322 Free PMC article.
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