rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
12
|
pubmed:dateCreated |
2007-1-17
|
pubmed:abstractText |
Germline mutation in adenomatous polyposis coli (APC) is detected in up to 80% of familial adenomatous polyposis (FAP) patients worldwide. In this study, we evaluated clinical features and APC mutations of Singapore FAP patients and contrasted genotype-phenotype correlation with Caucasians from other regions of the world and between FAP patients with and without detectable APC mutations.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0002-9270
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
101
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2810-7
|
pubmed:meshHeading |
pubmed-meshheading:17026565-Adenomatous Polyposis Coli,
pubmed-meshheading:17026565-Adult,
pubmed-meshheading:17026565-Aged,
pubmed-meshheading:17026565-Asian Continental Ancestry Group,
pubmed-meshheading:17026565-Colorectal Neoplasms,
pubmed-meshheading:17026565-Female,
pubmed-meshheading:17026565-Genes, APC,
pubmed-meshheading:17026565-Genotype,
pubmed-meshheading:17026565-Germ-Line Mutation,
pubmed-meshheading:17026565-Humans,
pubmed-meshheading:17026565-Male,
pubmed-meshheading:17026565-Middle Aged,
pubmed-meshheading:17026565-Phenotype,
pubmed-meshheading:17026565-Singapore
|
pubmed:year |
2006
|
pubmed:articleTitle |
Singapore familial adenomatous polyposis (FAP) patients with classical adenomatous polyposis but undetectable APC mutations have accelerated cancer progression.
|
pubmed:affiliation |
Department of Colorectal Surgery, Singapore General Hospital, Singapore.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|