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

Year Number of Results
1980 1
1982 2
1983 1
1985 1
1988 1
1989 2
1990 1
1991 3
1992 2
1993 6
1994 2
1995 2
1996 1
1997 3
1998 9
1999 13
2000 6
2001 15
2002 9
2003 7
2004 13
2005 17
2006 14
2007 18
2008 18
2009 17
2010 20
2011 24
2012 25
2013 31
2014 38
2015 29
2016 37
2017 34
2018 30
2019 31
2020 47
2021 42
2022 38
2023 53
2024 23

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PubMed for id: 342070

600 results

Results by year

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Page 1
The Skeleton of Lateral Meningocele Syndrome.
Canalis E. Canalis E. Front Genet. 2021 Jan 14;11:620334. doi: 10.3389/fgene.2020.620334. eCollection 2020. Front Genet. 2021. PMID: 33519922 Free PMC article. Review.
Expansion of the phenotype of lateral meningocele syndrome.
Cappuccio G, Apuzzo D, Alagia M, Torella A, Pinelli M, Franco B, Corrado B, Del Giudice E, D'Amico A, Nigro V; TUDP; Brunetti-Pierri N. Cappuccio G, et al. Am J Med Genet A. 2020 May;182(5):1259-1262. doi: 10.1002/ajmg.a.61536. Epub 2020 Mar 6. Am J Med Genet A. 2020. PMID: 32141180 Free PMC article.
NOTCH3-Related Lateral Meningocele Syndrome.
Ejaz R, Carter M, Gripp K. Ejaz R, et al. 2016 Jun 23 [updated 2022 May 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2016 Jun 23 [updated 2022 May 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 27336130 Free Books & Documents. Review.
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome.
Gripp KW, Robbins KM, Sobreira NL, Witmer PD, Bird LM, Avela K, Makitie O, Alves D, Hogue JS, Zackai EH, Doheny KF, Stabley DL, Sol-Church K. Gripp KW, et al. Am J Med Genet A. 2015 Feb;167A(2):271-81. doi: 10.1002/ajmg.a.36863. Epub 2014 Nov 13. Am J Med Genet A. 2015. PMID: 25394726 Free PMC article.
600 results