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pubmed-article:14614243pubmed:abstractTextModelling of variation in identical-by-descent (IBD) allele sharing using covariates can increase power to detect linkage, identify covariate-defined subgroups linked to particular marker regions, and improve the design of subsequent studies to localize genes and characterize their effects. In this report, we highlight issues that arise in studies of families with affected relatives.lld:pubmed
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pubmed-article:14614243pubmed:authorpubmed-author:BullShelley...lld:pubmed
pubmed-article:14614243pubmed:authorpubmed-author:LoganAlexande...lld:pubmed
pubmed-article:14614243pubmed:authorpubmed-author:HenneThomasTlld:pubmed
pubmed-article:14614243pubmed:authorpubmed-author:MireaLuciaLlld:pubmed
pubmed-article:14614243pubmed:copyrightInfoCopyright 2003 S. Karger AG, Basellld:pubmed
pubmed-article:14614243pubmed:issnTypePrintlld:pubmed
pubmed-article:14614243pubmed:volume56lld:pubmed
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pubmed-article:14614243pubmed:pagination94-106lld:pubmed
pubmed-article:14614243pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:14614243pubmed:year2003lld:pubmed
pubmed-article:14614243pubmed:articleTitleHeterogeneity in IBD allele sharing among covariate-defined subgroups: issues and findings for affected relatives.lld:pubmed
pubmed-article:14614243pubmed:affiliationSamuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ont., Canada. bull@mshri.on.calld:pubmed
pubmed-article:14614243pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:14614243pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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