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

Year Number of Results
1991 4
1994 2
1995 2
1996 2
1997 3
1998 4
2000 5
2001 7
2002 14
2003 7
2004 9
2005 11
2006 11
2007 12
2008 11
2009 17
2010 18
2011 20
2012 18
2013 11
2014 15
2015 13
2016 10
2017 13
2018 13
2019 19
2020 27
2021 20
2022 12
2023 11
2024 1

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PubMed for id: 51176

313 results

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Page 1
Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling.
Dufour W, Alawbathani S, Jourdain AS, Asif M, Baujat G, Becker C, Budde B, Gallacher L, Georgomanolis T, Ghoumid J, Höhne W, Lyonnet S, Ba-Saddik IA, Manouvrier-Hanu S, Motameny S, Noegel AA, Pais L, Vanlerberghe C, Wagle P, White SM, Willems M, Nürnberg P, Escande F, Petit F, Hussain MS. Dufour W, et al. Genet Med. 2022 Aug;24(8):1708-1721. doi: 10.1016/j.gim.2022.04.022. Epub 2022 May 18. Genet Med. 2022. PMID: 35583550 Free article.
313 results