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

Year Number of Results
1994 1
1995 1
1997 1
1999 2
2000 1
2001 1
2002 3
2003 4
2004 4
2006 1
2007 2
2008 4
2009 2
2010 7
2011 4
2012 3
2013 2
2014 9
2015 7
2016 7
2017 7
2018 4
2019 12
2020 3
2021 1
2022 1
2024 0

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Similar articles for PMID: 31649781

83 results

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Page 1
Chiari Malformation Type I in a Patient with a Novel NKX2-1 Mutation.
Gonçalves D, Lourenço L, Guardiano M, Castro-Correia C, Sampaio M, Leão M. Gonçalves D, et al. J Pediatr Neurosci. 2019 Jul-Sep;14(3):169-172. doi: 10.4103/jpn.JPN_108_18. Epub 2019 Sep 27. J Pediatr Neurosci. 2019. PMID: 31649781 Free PMC article.
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.
Thorwarth A, Schnittert-Hübener S, Schrumpf P, Müller I, Jyrch S, Dame C, Biebermann H, Kleinau G, Katchanov J, Schuelke M, Ebert G, Steininger A, Bönnemann C, Brockmann K, Christen HJ, Crock P, deZegher F, Griese M, Hewitt J, Ivarsson S, Hübner C, Kapelari K, Plecko B, Rating D, Stoeva I, Ropers HH, Grüters A, Ullmann R, Krude H. Thorwarth A, et al. J Med Genet. 2014 Jun;51(6):375-87. doi: 10.1136/jmedgenet-2013-102248. Epub 2014 Apr 8. J Med Genet. 2014. PMID: 24714694 Free PMC article.
83 results