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Deciphering the mutational signature of congenital limb malformations.
Sun L, Huang Y, Zhao S, Zhao J, Yan Z, Guo Y, Lin M, Zhong W, Yin Y, Chen Z, Zhang N, Zhang Y, Zhao Z, Li Q, Wang L, Dong X, Li Y, Li X, Qiu G; DISCO (Deciphering Disorders Involving Scoliosis & COmorbidities) study group; Zhang TJ, Wu Z, Tian W, Wu N. Sun L, et al. Among authors: li y, li x, li q. Mol Ther Nucleic Acids. 2021 Apr 20;24:961-970. doi: 10.1016/j.omtn.2021.04.012. eCollection 2021 Jun 4. Mol Ther Nucleic Acids. 2021. PMID: 34094714 Free PMC article.
Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly.
Sun L, Huang Y, Zhao S, Zhong W, Shi J, Guo Y, Zhao J, Xiong G, Yin Y, Chen Z, Zhang N, Zhao Z, Li Q, Chen D, Niu Y, Li X, Qiu G, Wu Z, Zhang TJ, Tian W, Wu N. Sun L, et al. Among authors: li x, li q. Front Genet. 2022 Mar 10;13:804202. doi: 10.3389/fgene.2022.804202. eCollection 2022. Front Genet. 2022. PMID: 35360850 Free PMC article.
Spectrum of Spondyloarthritis Among Chinese Populations.
Zhang S, Peng L, Li Q, Zhao J, Xu D, Zhao J, Wang Q, Li M, Zhang W, Tian X, Su J, Zeng X. Zhang S, et al. Among authors: li m, li q. Curr Rheumatol Rep. 2022 Aug;24(8):247-258. doi: 10.1007/s11926-022-01079-1. Epub 2022 Jul 13. Curr Rheumatol Rep. 2022. PMID: 35829981 Free PMC article. Review.
CRISPR-Based Tools for Fighting Rare Diseases.
Li Q, Gao Y, Wang H. Li Q, et al. Life (Basel). 2022 Nov 24;12(12):1968. doi: 10.3390/life12121968. Life (Basel). 2022. PMID: 36556333 Free PMC article. Review.
66,370 results
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