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pubmed-article:16858072pubmed:issue9lld:pubmed
pubmed-article:16858072pubmed:dateCreated2006-8-30lld:pubmed
pubmed-article:16858072pubmed:abstractTextInvestigation of the genetic background of complex traits is the focus of recent interest, as several common diseases or the individual response to treatments of various illnesses have not yet been explored. These studies require the development and implementation of reliable and large-scale genotyping methods. In this report, we introduce an efficient technique based on PCR-restriction fragment length sequence variation technique for the analysis of the -360CG and -201CT single-nucleotide sequence variations in the deoxycytidine kinase gene.lld:pubmed
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pubmed-article:16858072pubmed:authorpubmed-author:RonaiZsoltZlld:pubmed
pubmed-article:16858072pubmed:authorpubmed-author:Sasvari-Szeke...lld:pubmed
pubmed-article:16858072pubmed:authorpubmed-author:BonnGüntherGlld:pubmed
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pubmed-article:16858072pubmed:pagination1756-62lld:pubmed
pubmed-article:16858072pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:16858072pubmed:year2006lld:pubmed
pubmed-article:16858072pubmed:articleTitleMulticapillary electrophoresis analysis of single-nucleotide sequence variations in the deoxycytidine kinase gene.lld:pubmed
pubmed-article:16858072pubmed:affiliationHorváth Laboratory of Bioseparation Sciences and Institute of Analytical Chemistry and Radiochemistry, Institute of Analytical Chemistry and Radiochemistry, Leopold-Franzens University, Innsbruck, Austria.lld:pubmed
pubmed-article:16858072pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16858072pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:16858072pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed