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

Year Number of Results
2000 1
2003 2
2004 1
2005 1
2006 2
2008 2
2009 1
2010 1
2012 2
2015 1
2017 2
2018 2
2019 3
2020 1
2023 1
2024 2

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Page 1
The congenital cranial dysinnervation disorders.
Gutowski NJ, Chilton JK. Gutowski NJ, et al. Among authors: chilton jk. Arch Dis Child. 2015 Jul;100(7):678-81. doi: 10.1136/archdischild-2014-307035. Epub 2015 Jan 29. Arch Dis Child. 2015. PMID: 25633065 Review.
Molecular mechanisms of axon guidance.
Chilton JK. Chilton JK. Dev Biol. 2006 Apr 1;292(1):13-24. doi: 10.1016/j.ydbio.2005.12.048. Epub 2006 Feb 14. Dev Biol. 2006. PMID: 16476423 Free article. Review.
Copy number variation of LINGO1 in familial dystonic tremor.
Alakbarzade V, Iype T, Chioza BA, Singh R, Harlalka GV, Hardy H, Sreekantan-Nair A, Proukakis C, Peall K, Clark LN, Caswell R, Lango Allen H, Wakeling M, Chilton JK, Baple EL, Louis ED, Warner TT, Crosby AH. Alakbarzade V, et al. Among authors: chilton jk. Neurol Genet. 2019 Feb 4;5(1):e307. doi: 10.1212/NXG.0000000000000307. eCollection 2019 Feb. Neurol Genet. 2019. PMID: 30842974 Free PMC article.
Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies.
Salter CG, Beijer D, Hardy H, Barwick KES, Bower M, Mademan I, De Jonghe P, Deconinck T, Russell MA, McEntagart MM, Chioza BA, Blakely RD, Chilton JK, De Bleecker J, Baets J, Baple EL, Walk D, Crosby AH. Salter CG, et al. Among authors: chilton jk. Neurol Genet. 2018 Mar 23;4(2):e222. doi: 10.1212/NXG.0000000000000222. eCollection 2018 Apr. Neurol Genet. 2018. PMID: 29582019 Free PMC article.
22 results