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Year | Number of Results |
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2004 | 1 |
2005 | 1 |
2007 | 1 |
2024 | 0 |
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Spectrum of genetic alterations in Muir-Torre syndrome is the same as in HNPCC.
Am J Med Genet A. 2004 Mar 15;125A(3):318-9. doi: 10.1002/ajmg.a.20523.
Am J Med Genet A. 2004.
PMID: 14994245
No abstract available.
Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC.
Stella A, Surdo NC, Lastella P, Barana D, Oliani C, Tibiletti MG, Viel A, Natale C, Piepoli A, Marra G, Guanti G.
Stella A, et al.
Clin Genet. 2007 Feb;71(2):130-9. doi: 10.1111/j.1399-0004.2007.00745.x.
Clin Genet. 2007.
PMID: 17250661
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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).
van der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, Delozier-Blanchet C, Hutter P, Foulkes W, Lynch H, Burn J, Möslein G, Fodde R.
van der Klift H, et al.
Genes Chromosomes Cancer. 2005 Oct;44(2):123-38. doi: 10.1002/gcc.20219.
Genes Chromosomes Cancer. 2005.
PMID: 15942939
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