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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2003-11-5
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pubmed:abstractText |
Prostate cancer (CaP) is a common disorder with multiple genetic and environmental factors contributing to the disease. CaP susceptibility loci can be identified through genome-wide scans of high-risk families.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0270-4137
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pubmed:author |
pubmed-author:AlbertusJulie AJA,
pubmed-author:BerghAndersA,
pubmed-author:DamberJan-ErikJE,
pubmed-author:EmanuelssonMonicaM,
pubmed-author:Freas-LutzDiana LDL,
pubmed-author:GöranssonIngelaI,
pubmed-author:GildeaDerek EDE,
pubmed-author:GillandersElizabeth MEM,
pubmed-author:GrönbergHenrikH,
pubmed-author:JonesMaryPat SMS,
pubmed-author:JonssonBjörn-AndersBA,
pubmed-author:LindmarkFredrikF,
pubmed-author:MarkeyCarol JCJ,
pubmed-author:RiedeselErica LEL,
pubmed-author:StenmanElisabethE,
pubmed-author:TrentJeffry MJM,
pubmed-author:WiklundFredrikF
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pubmed:copyrightInfo |
Copyright 2003 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
57
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
290-7
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:14601025-Aged,
pubmed-meshheading:14601025-Alleles,
pubmed-meshheading:14601025-Chromosomes, Human, Pair 19,
pubmed-meshheading:14601025-Chromosomes, Human, Pair 5,
pubmed-meshheading:14601025-DNA, Neoplasm,
pubmed-meshheading:14601025-Family,
pubmed-meshheading:14601025-Female,
pubmed-meshheading:14601025-Genetic Linkage,
pubmed-meshheading:14601025-Genetic Predisposition to Disease,
pubmed-meshheading:14601025-Genome, Human,
pubmed-meshheading:14601025-Humans,
pubmed-meshheading:14601025-Male,
pubmed-meshheading:14601025-Middle Aged,
pubmed-meshheading:14601025-Polymerase Chain Reaction,
pubmed-meshheading:14601025-Prostatic Neoplasms,
pubmed-meshheading:14601025-Sequence Analysis, DNA,
pubmed-meshheading:14601025-Statistics, Nonparametric,
pubmed-meshheading:14601025-Sweden
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pubmed:year |
2003
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pubmed:articleTitle |
Genome-wide scan of Swedish families with hereditary prostate cancer: suggestive evidence of linkage at 5q11.2 and 19p13.3.
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pubmed:affiliation |
Department of Radiation Sciences, Oncology, University of Umeå, Umeå, Sweden. fredrik.wiklund@oc.umu.se
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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