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

Year Number of Results
1982 2
1984 1
1985 4
1986 2
1987 2
1989 1
1990 1
1991 3
1992 3
1993 6
1994 3
1995 10
1996 12
1997 15
1998 12
1999 7
2000 16
2001 4
2002 3
2003 5
2004 2
2005 11
2006 5
2008 3
2009 5
2010 4
2011 4
2012 8
2013 3
2014 5
2015 6
2016 4
2017 5
2018 5
2019 2
2020 4
2021 5
2022 4
2023 1
2024 0

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Similar articles for PMID: 8841187

191 results

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Page 1
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, Komoto Y, Okada A, Ohishi S, Nabetani A, Morisaki H, Nakayama M, Niikawa N, Mukai T. Hatada I, et al. Nat Genet. 1996 Oct;14(2):171-3. doi: 10.1038/ng1096-171. Nat Genet. 1996. PMID: 8841187
p57K1P2 is expressed in Wilms' tumor with LOH of 11p15.5.
Overall ML, Spencer J, Bakker M, Dziadek M, Smith PJ. Overall ML, et al. Genes Chromosomes Cancer. 1996 Sep;17(1):56-9. doi: 10.1002/(SICI)1098-2264(199609)17:1<56::AID-GCC8>3.0.CO;2-1. Genes Chromosomes Cancer. 1996. PMID: 8889507
191 results