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

Year Number of Results
1986 1
1989 2
1990 1
1992 2
1995 1
1996 1
1997 1
2001 2
2004 1
2005 1
2008 1
2009 1
2010 2
2011 2
2012 1
2013 1
2014 1
2015 1
2016 2
2017 1
2024 0

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23 results

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Page 1
Familial Wilms tumor.
Ruteshouser EC, Huff V. Ruteshouser EC, et al. Am J Med Genet C Semin Med Genet. 2004 Aug 15;129C(1):29-34. doi: 10.1002/ajmg.c.30025. Am J Med Genet C Semin Med Genet. 2004. PMID: 15264270 Review.
Absence of PPP2R1A mutations in Wilms tumor.
Ruteshouser EC, Ashworth LK, Huff V. Ruteshouser EC, et al. Oncogene. 2001 Apr 12;20(16):2050-4. doi: 10.1038/sj.onc.1204301. Oncogene. 2001. PMID: 11360189
Rare variant detection using family-based sequencing analysis.
Peng G, Fan Y, Palculict TB, Shen P, Ruteshouser EC, Chi AK, Davis RW, Huff V, Scharfe C, Wang W. Peng G, et al. Among authors: ruteshouser ec. Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):3985-90. doi: 10.1073/pnas.1222158110. Epub 2013 Feb 20. Proc Natl Acad Sci U S A. 2013. PMID: 23426633 Free PMC article.
Loss of heterozygosity at 2q37 in sporadic Wilms' tumor: putative role for miR-562.
Drake KM, Ruteshouser EC, Natrajan R, Harbor P, Wegert J, Gessler M, Pritchard-Jones K, Grundy P, Dome J, Huff V, Jones C, Aldred MA. Drake KM, et al. Among authors: ruteshouser ec. Clin Cancer Res. 2009 Oct 1;15(19):5985-92. doi: 10.1158/1078-0432.CCR-09-1065. Epub 2009 Sep 29. Clin Cancer Res. 2009. PMID: 19789318 Free PMC article.
23 results