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

Year Number of Results
1987 2
1988 1
1989 1
1990 2
1994 3
1995 2
1996 5
1997 2
1998 3
1999 4
2000 5
2001 8
2002 5
2003 2
2004 1
2005 4
2006 5
2007 2
2008 2
2009 2
2010 3
2011 6
2012 4
2013 3
2014 1
2015 3
2016 4
2017 2
2018 1
2019 1
2026 0

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85 results

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Page 1
Molecular etiology of factor VIII deficiency in hemophilia A.
Antonarakis SE, Kazazian HH, Gitschier J, Hutter P, de Moerloose P, Morris MA. Antonarakis SE, et al. Among authors: hutter p. Adv Exp Med Biol. 1995;386:19-34. doi: 10.1007/978-1-4613-0331-2_2. Adv Exp Med Biol. 1995. PMID: 8851012 Review. No abstract available.
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study.
Kempers MJ, Kuiper RP, Ockeloen CW, Chappuis PO, Hutter P, Rahner N, Schackert HK, Steinke V, Holinski-Feder E, Morak M, Kloor M, Büttner R, Verwiel ET, van Krieken JH, Nagtegaal ID, Goossens M, van der Post RS, Niessen RC, Sijmons RH, Kluijt I, Hogervorst FB, Leter EM, Gille JJ, Aalfs CM, Redeker EJ, Hes FJ, Tops CM, van Nesselrooij BP, van Gijn ME, Gómez García EB, Eccles DM, Bunyan DJ, Syngal S, Stoffel EM, Culver JO, Palomares MR, Graham T, Velsher L, Papp J, Oláh E, Chan TL, Leung SY, van Kessel AG, Kiemeney LA, Hoogerbrugge N, Ligtenberg MJ. Kempers MJ, et al. Among authors: hutter p. Lancet Oncol. 2011 Jan;12(1):49-55. doi: 10.1016/S1470-2045(10)70265-5. Epub 2010 Dec 8. Lancet Oncol. 2011. PMID: 21145788 Free PMC article.
[Multidisciplinary management of hereditary colorectal cancer].
Soravia C, Delozier-Blanchet C, Blouin JL, Bründler MA, Egger JF, Queneau PE, Roth AD, Marti MC, Antonarakis SE, Morel P, Hutter P. Soravia C, et al. Among authors: hutter p. Swiss Surg. 2001;7(3):99-104. doi: 10.1024/1023-9332.7.3.99. Swiss Surg. 2001. PMID: 11407044 French.
Prediction of dementia in primary care patients.
Jessen F, Wiese B, Bickel H, Eiffländer-Gorfer S, Fuchs A, Kaduszkiewicz H, Köhler M, Luck T, Mösch E, Pentzek M, Riedel-Heller SG, Wagner M, Weyerer S, Maier W, van den Bussche H; AgeCoDe Study Group. Jessen F, et al. PLoS One. 2011 Feb 18;6(2):e16852. doi: 10.1371/journal.pone.0016852. PLoS One. 2011. PMID: 21364746 Free PMC article.
Recurrence and variability of germline EPCAM deletions in Lynch syndrome.
Kuiper RP, Vissers LE, Venkatachalam R, Bodmer D, Hoenselaar E, Goossens M, Haufe A, Kamping E, Niessen RC, Hogervorst FB, Gille JJ, Redeker B, Tops CM, van Gijn ME, van den Ouweland AM, Rahner N, Steinke V, Kahl P, Holinski-Feder E, Morak M, Kloor M, Stemmler S, Betz B, Hutter P, Bunyan DJ, Syngal S, Culver JO, Graham T, Chan TL, Nagtegaal ID, van Krieken JH, Schackert HK, Hoogerbrugge N, van Kessel AG, Ligtenberg MJ. Kuiper RP, et al. Among authors: hutter p. Hum Mutat. 2011 Apr;32(4):407-14. doi: 10.1002/humu.21446. Epub 2011 Mar 1. Hum Mutat. 2011. PMID: 21309036
85 results