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pubmed-article:1472385pubmed:abstractTextThis article describes a method for determining whether a particular nucleic acid sequence is present in a sample and for discriminating between any two nucleic acid sequences if such sequences differ only by a single nucleotide. The method entails extension of a novel two-component primer on templates that may or may not include a target nucleic acid sequence. The 3' portion of the primer is complementary to a portion of the template adjacent to the target sequence (for example, the polymorphic nucleotide). The 5' portion of the primer is complementary to a different preselected nucleic acid sequence. Extension of the 3' portion of the primer with a labeled deoxynucleoside triphosphate yields a labeled extension product, but only if the template includes the target sequence. The presence of such a labeled primer-extension product is detected by hybridization of the 5' portion to the preselected sequence. The preselected sequence is immobilized on a solid support. The method has been applied to genotyping individuals for the two-allele polymorphism of the human tyrosinase gene.lld:pubmed
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pubmed-article:1472385pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:1472385pubmed:articleTitleDetection of specific alleles by using allele-specific primer extension followed by capture on solid support.lld:pubmed
pubmed-article:1472385pubmed:affiliationDepartment of Molecular Biochemistry, Beckman Research Institute of the City of Hope, Duarte, California.lld:pubmed
pubmed-article:1472385pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1472385pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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