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Results by year

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

Year Number of Results
1998 3
1999 8
2000 7
2001 5
2002 3
2003 6
2004 6
2005 6
2006 6
2007 6
2008 1
2009 6
2010 6
2011 10
2012 7
2013 10
2014 6
2015 2
2016 4
2017 5
2018 3
2019 3
2020 5
2021 1
2022 2
2023 2
2024 0

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Similar articles for PMID: 16648371

117 results

Results by year

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Page 1
Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.
de Leng WW, Jansen M, Carvalho R, Polak M, Musler AR, Milne AN, Keller JJ, Menko FH, de Rooij FW, Iacobuzio-Donahue CA, Giardiello FM, Weterman MA, Offerhaus GJ. de Leng WW, et al. Clin Genet. 2007 Dec;72(6):568-73. doi: 10.1111/j.1399-0004.2007.00907.x. Epub 2007 Oct 9. Clin Genet. 2007. PMID: 17924967 Free PMC article.
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
Hearle NC, Rudd MF, Lim W, Murday V, Lim AG, Phillips RK, Lee PW, O'donohue J, Morrison PJ, Norman A, Hodgson SV, Lucassen A, Houlston RS. Hearle NC, et al. J Med Genet. 2006 Apr;43(4):e15. doi: 10.1136/jmg.2005.036830. J Med Genet. 2006. PMID: 16582077 Free PMC article.
117 results