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

Year Number of Results
1988 1
1991 1
1994 1
1996 1
1997 1
1998 2
1999 2
2000 4
2001 4
2002 10
2003 4
2004 4
2005 4
2006 6
2007 7
2008 8
2009 6
2010 10
2011 12
2012 11
2013 11
2014 8
2015 8
2016 7
2017 5
2018 9
2019 5
2020 8
2021 11
2022 10
2023 5
2024 0

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Similar articles for PMID: 18326838

167 results

Results by year

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Page 1
DLX5, FGF8 and the Pin1 isomerase control ΔNp63α protein stability during limb development: a regulatory loop at the basis of the SHFM and EEC congenital malformations.
Restelli M, Lopardo T, Lo Iacono N, Garaffo G, Conte D, Rustighi A, Napoli M, Del Sal G, Perez-Morga D, Costanzo A, Merlo GR, Guerrini L. Restelli M, et al. Hum Mol Genet. 2014 Jul 15;23(14):3830-42. doi: 10.1093/hmg/ddu096. Epub 2014 Feb 25. Hum Mol Genet. 2014. PMID: 24569166 Free PMC article.
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.
van Bokhoven H, Hamel BC, Bamshad M, Sangiorgi E, Gurrieri F, Duijf PH, Vanmolkot KR, van Beusekom E, van Beersum SE, Celli J, Merkx GF, Tenconi R, Fryns JP, Verloes A, Newbury-Ecob RA, Raas-Rotschild A, Majewski F, Beemer FA, Janecke A, Chitayat D, Crisponi G, Kayserili H, Yates JR, Neri G, Brunner HG. van Bokhoven H, et al. Am J Hum Genet. 2001 Sep;69(3):481-92. doi: 10.1086/323123. Epub 2001 Jul 17. Am J Hum Genet. 2001. PMID: 11462173 Free PMC article.
167 results