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Results by year

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

Year Number of Results
1984 2
1985 2
1986 1
1988 1
1989 2
1990 1
1991 3
1992 1
1993 1
1994 2
1995 6
1996 2
1997 3
1998 6
1999 1
2000 3
2001 2
2002 2
2003 1
2004 2
2005 5
2006 3
2007 1
2008 4
2009 4
2010 2
2011 1
2012 6
2013 5
2014 4
2015 9
2016 6
2017 3
2018 6
2020 3
2021 3
2022 5
2023 1
2024 0

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Similar articles for PMID: 18780370

106 results

Results by year

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Page 1
Perlman syndrome: report, prenatal findings and review.
Alessandri JL, Cuillier F, Ramful D, Ernould S, Robin S, de Napoli-Cocci S, Rivière JP, Rossignol S. Alessandri JL, et al. Am J Med Genet A. 2008 Oct 1;146A(19):2532-7. doi: 10.1002/ajmg.a.32391. Am J Med Genet A. 2008. PMID: 18780370 Review.
The Perlman familial nephroblastomatosis syndrome.
Greenberg F, Stein F, Gresik MV, Finegold MJ, Carpenter RJ, Riccardi VM, Beaudet AL. Greenberg F, et al. Am J Med Genet. 1986 May;24(1):101-10. doi: 10.1002/ajmg.1320240112. Am J Med Genet. 1986. PMID: 3010722
Perlman syndrome: four additional cases and review.
Henneveld HT, van Lingen RA, Hamel BC, Stolte-Dijkstra I, van Essen AJ. Henneveld HT, et al. Am J Med Genet. 1999 Oct 29;86(5):439-46. Am J Med Genet. 1999. PMID: 10508986 Review.
[Perlman syndrome research progress].
Wang Z, Liu J, Yang Y. Wang Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Oct 10;38(10):1021-1024. doi: 10.3760/cma.j.cn511374-20200717-00525. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34625946 Chinese.
Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.
Isidor B, Bourdeaut F, Lafon D, Plessis G, Lacaze E, Kannengiesser C, Rossignol S, Pichon O, Briand A, Martin-Coignard D, Piccione M, David A, Delattre O, Jeanpierre C, Sévenet N, Le Caignec C. Isidor B, et al. Eur J Hum Genet. 2013 Jul;21(7):784-7. doi: 10.1038/ejhg.2012.252. Epub 2012 Nov 21. Eur J Hum Genet. 2013. PMID: 23169491 Free PMC article.
106 results