Source:http://linkedlifedata.com/resource/pubmed/id/17238184
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2007-2-12
|
pubmed:abstractText |
Most individuals with Familial Adenomatous Polyposis (FAP) harbor mutations in the APC gene on chromosome 5q21. They are at an increased risk of brain tumors, including cerebellar medulloblastoma, when compared with the general population (Brain Tumor Polyposis-BTP Type 2). Genotype-phenotype correlations between APC gene mutations and central nervous system (CNS) tumors have, thus far not been successful. Herein the authors have pooled their registry experience in BTP type 2 with the published reports.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0008-543X
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
109
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
761-6
|
pubmed:meshHeading |
pubmed-meshheading:17238184-Adenomatous Polyposis Coli,
pubmed-meshheading:17238184-Adenomatous Polyposis Coli Protein,
pubmed-meshheading:17238184-Adolescent,
pubmed-meshheading:17238184-Adult,
pubmed-meshheading:17238184-Brain Neoplasms,
pubmed-meshheading:17238184-Child,
pubmed-meshheading:17238184-Codon,
pubmed-meshheading:17238184-Female,
pubmed-meshheading:17238184-Humans,
pubmed-meshheading:17238184-Male,
pubmed-meshheading:17238184-Mutation,
pubmed-meshheading:17238184-Pedigree,
pubmed-meshheading:17238184-Registries
|
pubmed:year |
2007
|
pubmed:articleTitle |
Brain tumors in individuals with familial adenomatous polyposis: a cancer registry experience and pooled case report analysis.
|
pubmed:affiliation |
Department of Pediatrics, University of Nebraska Medical Center, Creighton University School of Medicine, Omaha, Nebraska 68198, USA. tattard@unmc.edu
|
pubmed:publicationType |
Meta-Analysis
|