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

Year Number of Results
1996 1
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1999 11
2000 4
2001 3
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2004 7
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2006 6
2007 5
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2009 9
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2011 8
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2020 8
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Similar articles for PMID: 15121768

175 results

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Page 1
Genotype-phenotype correlations in Peutz-Jeghers syndrome.
Amos CI, Keitheri-Cheteri MB, Sabripour M, Wei C, McGarrity TJ, Seldin MF, Nations L, Lynch PM, Fidder HH, Friedman E, Frazier ML. Amos CI, et al. J Med Genet. 2004 May;41(5):327-33. doi: 10.1136/jmg.2003.010900. J Med Genet. 2004. PMID: 15121768 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.
STK11 status and intussusception risk in Peutz-Jeghers syndrome.
Hearle N, Schumacher V, Menko FH, Olschwang S, Boardman LA, Gille JJ, Keller JJ, Westerman AM, Scott RJ, Lim W, Trimbath JD, Giardiello FM, Gruber SB, Offerhaus GJ, Rooij FW, Wilson JH, Hansmann A, Möslein G, Royer-Pokora B, Vogel T, Phillips RK, Spigelman AD, Houlston RS. Hearle N, et al. J Med Genet. 2006 Aug;43(8):e41. doi: 10.1136/jmg.2005.040535. J Med Genet. 2006. PMID: 16882735 Free PMC article.
175 results