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

Year Number of Results
1990 1
1991 2
1992 1
1993 2
1995 1
1996 1
1997 2
1999 1
2003 1
2004 2
2006 5
2007 3
2008 3
2009 2
2010 1
2011 3
2012 3
2013 7
2014 4
2015 2
2017 2
2018 3
2019 1
2020 2
2021 1
2022 2
2023 1
2024 0

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54 results

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Page 1
NF1 Somatic Mutation in Dystrophic Scoliosis.
Margraf RL, VanSant-Webb C, Mao R, Viskochil DH, Carey J, Hanson H, D'Astous J, Grossmann A, Stevenson DA. Margraf RL, et al. J Mol Neurosci. 2019 May;68(1):11-18. doi: 10.1007/s12031-019-01277-0. Epub 2019 Feb 18. J Mol Neurosci. 2019. PMID: 30778836
Genetic Variants Associated with Port-Wine Stains.
Frigerio A, Wright K, Wooderchak-Donahue W, Tan OT, Margraf R, Stevenson DA, Grimmer JF, Bayrak-Toydemir P. Frigerio A, et al. Among authors: margraf r. PLoS One. 2015 Jul 20;10(7):e0133158. doi: 10.1371/journal.pone.0133158. eCollection 2015. PLoS One. 2015. PMID: 26192947 Free PMC article.
TACI mutation p.Lys154Ter identified in Good Syndrome.
Margraf RL, Coonrod EM, Durtschi JD, Augustine NH, Voelkerding KV, Hill HR, Kumánovics A. Margraf RL, et al. Clin Immunol. 2013 Jan;146(1):10-2. doi: 10.1016/j.clim.2012.10.006. Epub 2012 Oct 31. Clin Immunol. 2013. PMID: 23165285 No abstract available.
Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia.
Wooderchak-Donahue WL, McDonald J, Farrell A, Akay G, Velinder M, Johnson P, VanSant-Webb C, Margraf R, Briggs E, Whitehead KJ, Thomson J, Lin AE, Pyeritz RE, Marth G, Bayrak-Toydemir P. Wooderchak-Donahue WL, et al. Among authors: margraf r. J Med Genet. 2018 Dec;55(12):824-830. doi: 10.1136/jmedgenet-2018-105561. Epub 2018 Sep 22. J Med Genet. 2018. PMID: 30244195
54 results