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

Year Number of Results
1993 6
1998 3
1999 1
2000 3
2001 1
2002 2
2003 3
2004 2
2005 4
2006 6
2007 5
2008 5
2009 4
2010 4
2011 7
2012 7
2013 12
2014 10
2015 7
2016 2
2017 4
2018 10
2019 10
2020 9
2021 14
2022 11
2023 4
2024 2

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PubMed for id: 4629

135 results

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Page 1
A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus.
Chesneau B, Plancke A, Rolland G, Marcheix B, Dulac Y, Edouard T, Plaisancié J, Aubert-Mucca M, Julia S, Langeois M, Lavabre-Bertrand T, Khau Van Kien P. Chesneau B, et al. Mol Genet Genomic Med. 2021 Nov;9(11):e1814. doi: 10.1002/mgg3.1814. Epub 2021 Oct 21. Mol Genet Genomic Med. 2021. PMID: 34672437 Free PMC article.
135 results