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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 8
2003 17
2004 10
2005 13
2006 20
2007 19
2008 16
2009 14
2010 14
2011 12
2012 13
2013 6
2014 12
2015 12
2016 4
2017 10
2018 10
2019 11
2020 6
2021 5
2022 3
2023 3
2024 0

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215 results

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Page 1
Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.
Tan D, Ge L, Fan Y, Chang X, Wang S, Wei C, Ding J, Liu A, Wang S, Li X, Gao K, Yang H, Que C, Huang Z, Li C, Zhu Y, Mao B, Jin B, Hua Y, Zhang X, Zhang B, Zhu W, Zhang C, Wang Y, Yuan Y, Jiang Y, Rutkowski A, Bönnemann CG, Wu X, Xiong H. Tan D, et al. Among authors: wu x. Orphanet J Rare Dis. 2021 Jul 19;16(1):319. doi: 10.1186/s13023-021-01950-x. Orphanet J Rare Dis. 2021. PMID: 34281576 Free PMC article.
Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients.
Fan Y, Tan D, Song D, Zhang X, Chang X, Wang Z, Zhang C, Chan SH, Wu Q, Wu L, Wang S, Yan H, Ge L, Yang H, Mao B, Bönnemann C, Liu J, Wang S, Yuan Y, Wu X, Zhang H, Xiong H. Fan Y, et al. Among authors: wu x. J Med Genet. 2021 May;58(5):326-333. doi: 10.1136/jmedgenet-2019-106671. Epub 2020 Jun 22. J Med Genet. 2021. PMID: 32571898 Free PMC article.
215 results