Familial Colorectal Cancer Type X

Known as: FCCTX 
Hereditary nonpolyposis colorectal cancer characterized by the absence of germline mutations in DNA mismatch-repair genes.
National Institutes of Health

Topic mentions per year

Topic mentions per year

2010-2016
02420102016

Papers overview

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2017
2017
Familiar colorectal cancer type X (FCCTX) comprises families that fulfill the Amsterdam criteria for hereditary non-polyposis… (More)
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Review
2015
Review
2015
Heredity is a major cause of colorectal cancer, but although several rare high-risk syndromes have been linked to disease… (More)
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2014
2014
Background:Familial Colorectal Cancer Type X (FCCTX) is defined as individuals with colorectal cancer (CRC) who families meet… (More)
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2014
2014
Familial colorectal cancer type X (FCCTX) is characterized by clinical features of hereditary non-polyposis colorectal cancer… (More)
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2014
2014
Familial colorectal cancer type X (FCCTX) fulfils clinical criteria defining Lynch syndrome (LS), but is not related to germline… (More)
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2013
2013
INTRODUCTION Heredity is estimated to cause at least 20% of colorectal cancer. The hereditary nonpolyposis colorectal cancer… (More)
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2013
2013
Lynch syndrome and familial colorectal cancer type X, FCCTX, represent the two predominant colorectal cancer syndromes. Whereas… (More)
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2012
2012
BACKGROUND The hereditary non-polyposis colorectal cancer (HNPCC) subset of tumours can broadly be divided into tumours caused by… (More)
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2011
2011
In a fraction of families fulfilling the Amsterdam criteria for hereditary non-polyposis colorectal cancer, colorectal cancers… (More)
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2010
2010
BACKGROUND AND AIMS Colorectal cancer (CRC) is the second most frequent cancer in developed countries. Newfoundland has the… (More)
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