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dc.rights.licenseCopyright law does not apply to Environmental Health Perspectives, which falls within the public domain.
dc.contributor.authorRyberg, D.en_US
dc.contributor.authorTefre, T.en_US
dc.contributor.authorSkaug, V.en_US
dc.contributor.authorStangeland, Lodveen_US
dc.contributor.authorØvrebø, S.en_US
dc.contributor.authorNaalsund, A.en_US
dc.contributor.authorBørresen, A.-L.en_US
dc.contributor.authorHaugen, Aa.en_US
dc.date.accessioned2016-06-21T13:47:31Z
dc.date.available2016-06-21T13:47:31Z
dc.date.issued1992-11
dc.PublishedEnvironmental Health Perspectives 1992, 98:187-189eng
dc.identifier.issn0091-6765
dc.identifier.urihttps://hdl.handle.net/1956/12156
dc.description.abstractWe have examined restriction fragment length polymorphisms of the H-ras-1 gene in germ-line DNA from 214 lung cancer patients and 309 unaffected controls. When DNA samples were digested with MspI/HpaII, Southern blot analysis revealed at least 22 different alleles, grouped according to their frequencies as common, intermediate, and rare. The frequency of rare alleles in lung cancer patients (16/428) is significantly different (p = 0.002) from that in the control group (5/618). Individuals with rare alleles were found to be at 4.7-fold greater risk of lung cancer than those with no rare alleles.en_US
dc.language.isoengeng
dc.publisherThe National Institute of Environmental Health Scienceseng
dc.titleAllele diversity of the H-ras-1 variable number of tandem repeats in Norwegian lung cancer patientsen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2016-04-07T08:15:37Z
dc.description.versionpublishedVersionen_US
dc.identifier.cristin388926
dc.subject.nsiVDP::Medisinske Fag: 700::Helsefag: 800en_US


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