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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

Papers overview

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2015
2015
Familial colorectal cancer type X (FCCX) encompasses a group of families with dominant inheritance pattern of colorectal cancer… Expand
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2014
2014
Familial colorectal cancer type X (FCCTX) is characterized by clinical features of hereditary non-polyposis colorectal cancer… Expand
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2014
2014
Background:Familial Colorectal Cancer Type X (FCCTX) is defined as individuals with colorectal cancer (CRC) who families meet… Expand
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2014
2014
Previous evidence indicates that mutations in the GALNT12 gene might cause a fraction of the unexplained familial colorectal… Expand
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Highly Cited
2014
Highly Cited
2014
Little is known about the genetic factors that contribute to familial colorectal cancer type X (FCCX), characterized by… Expand
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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… Expand
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2011
2011
In a fraction of families fulfilling the Amsterdam criteria for hereditary non-polyposis colorectal cancer, colorectal cancers… Expand
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Highly Cited
2010
Highly Cited
2010
BACKGROUND AND AIMS Colorectal cancer (CRC) is the second most frequent cancer in developed countries. Newfoundland has the… Expand
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Review
2009
Review
2009
Establishing the Amsterdam criteria, based on pedigrees, was essential for defining hereditary nonpolyposis colorectal cancer… Expand
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Highly Cited
2005
Highly Cited
2005
CONTEXT Approximately 60% of families that meet the Amsterdam-I criteria (AC-I) for hereditary nonpolyposis colorectal cancer… Expand
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