Genome-wide linkage analysis and tumoral characterization reveal heterogeneity in familial colorectal cancer type X
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology
Link
http://link.springer.com/content/pdf/10.1007/s00535-014-1009-0.pdf
Reference48 articles.
1. Lindor NM, Rabe K, Petersen GM, et al. Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X. JAMA. 2005;293:1979–85.
2. Jover R, Castells A. Molecular information defines a new entity of hereditary colorectal cancer. Gastroenterology. 2008;134:888–9 (Discussion 9–90).
3. Valle L, Perea J, Carbonell P, et al. Clinicopathologic and pedigree differences in Amsterdam I-positive hereditary nonpolyposis colorectal cancer families according to tumor microsatellite instability status. J Clin Oncol. 2007;25:781–6.
4. Llor X, Pons E, Xicola RM, et al. Differential features of colorectal cancers fulfilling Amsterdam criteria without involvement of the mutator pathway. Clin Cancer Res. 2005;11:7304–10.
5. Wiesner GL, Daley D, Lewis S, et al. A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2–31.2. Proc Natl Acad Sci USA. 2003;100:12961–5.
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