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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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Showing results for xiru wu
Search for Xiuru Wu instead (3 results)
Congenital muscular dystrophies in China.
Ge L, Zhang C, Wang Z, Chan SHS, Zhu W, Han C, Zhang X, Zheng H, Wu L, Jin B, Shan J, Mao B, Zhong J, Peng X, Cheng Y, Hu J, Sun Y, Lu J, Hua Y, Zhu S, Wei C, Wang S, Jiao H, Yang H, Fu X, Fan Y, Chang X, Wang S, Bao X, Zhang Y, Wang J, Wu Y, Jiang Y, Yuan Y, Rutkowski A, Bönnemann CG, Wei W, Wu X, Xiong H. Ge L, et al. Among authors: wu x. Clin Genet. 2019 Sep;96(3):207-215. doi: 10.1111/cge.13560. Epub 2019 Jun 6. Clin Genet. 2019. PMID: 31066047
GRIN2A mutations in epilepsy-aphasia spectrum disorders.
Yang X, Qian P, Xu X, Liu X, Wu X, Zhang Y, Yang Z. Yang X, et al. Among authors: wu x. Brain Dev. 2018 Mar;40(3):205-210. doi: 10.1016/j.braindev.2017.09.007. Epub 2017 Oct 19. Brain Dev. 2018. PMID: 29056244
CHD2-related epilepsy: novel mutations and new phenotypes.
Chen J, Zhang J, Liu A, Zhang L, Li H, Zeng Q, Yang Z, Yang X, Wu X, Zhang Y. Chen J, et al. Among authors: wu x. Dev Med Child Neurol. 2020 May;62(5):647-653. doi: 10.1111/dmcn.14367. Epub 2019 Nov 1. Dev Med Child Neurol. 2020. PMID: 31677157 Free article.
Mosaicism and incomplete penetrance of PCDH19 mutations.
Liu A, Yang X, Yang X, Wu Q, Zhang J, Sun D, Yang Z, Jiang Y, Wu X, Wei L, Zhang Y. Liu A, et al. Among authors: wu x. J Med Genet. 2019 Feb;56(2):81-88. doi: 10.1136/jmedgenet-2017-105235. Epub 2018 Oct 4. J Med Genet. 2019. PMID: 30287595 Free PMC article.
Familial cases and male cases with MECP2 mutations.
Zhang Q, Zhao Y, Bao X, Luo J, Zhang X, Li J, Wei L, Wu X. Zhang Q, et al. Among authors: wu x. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun;174(4):451-457. doi: 10.1002/ajmg.b.32534. Epub 2017 Apr 10. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28394482 Free PMC article.
215 results