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

Year Number of Results
1980 1
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1989 3
1990 2
1992 2
1993 3
1994 6
1995 5
1996 3
1997 3
1999 2
2000 4
2001 5
2002 2
2003 1
2004 1
2005 3
2007 1
2008 2
2009 3
2010 3
2011 3
2012 3
2013 1
2014 1
2015 3
2016 1
2017 3
2018 1
2019 1
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2023 1
2024 1

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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. Among authors: lavabre bertrand t. 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.
Parental mosaicism in Marfan and Ehlers-Danlos syndromes and related disorders.
Chesneau B, Plancke A, Rolland G, Chassaing N, Coubes C, Brischoux-Boucher E, Edouard T, Dulac Y, Aubert-Mucca M, Lavabre-Bertrand T, Plaisancié J, Khau Van Kien P. Chesneau B, et al. Among authors: lavabre bertrand t. Eur J Hum Genet. 2021 May;29(5):771-779. doi: 10.1038/s41431-020-00797-3. Epub 2021 Jan 7. Eur J Hum Genet. 2021. PMID: 33414558 Free PMC article.
Long non-coding RNAs in human early embryonic development and their potential in ART.
Bouckenheimer J, Assou S, Riquier S, Hou C, Philippe N, Sansac C, Lavabre-Bertrand T, Commes T, Lemaître JM, Boureux A, De Vos J. Bouckenheimer J, et al. Among authors: lavabre bertrand t. Hum Reprod Update. 2016 Dec;23(1):19-40. doi: 10.1093/humupd/dmw035. Epub 2016 Sep 21. Hum Reprod Update. 2016. PMID: 27655590 Review.
75 results