Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:3189402rdf:typepubmed:Citationlld:pubmed
pubmed-article:3189402lifeskim:mentionsumls-concept:C0041432lld:lifeskim
pubmed-article:3189402lifeskim:mentionsumls-concept:C0008633lld:lifeskim
pubmed-article:3189402lifeskim:mentionsumls-concept:C0004903lld:lifeskim
pubmed-article:3189402lifeskim:mentionsumls-concept:C0332197lld:lifeskim
pubmed-article:3189402lifeskim:mentionsumls-concept:C0262496lld:lifeskim
pubmed-article:3189402pubmed:issue3lld:pubmed
pubmed-article:3189402pubmed:dateCreated1988-12-7lld:pubmed
pubmed-article:3189402pubmed:abstractTextMonozygotic twins discordant for the Wiedemann-Beckwith syndrome (WBS) were studied by cytogenetic and molecular methods to determine if a genetic lesion could be detected in the affected child. Probes known to be localized on the short arm of chromosome 11 and a low copy-repetitive probe were used. No genetic lesions could be ascertained in normal or affected tissue obtained from the WBS twin.lld:pubmed
pubmed-article:3189402pubmed:languageenglld:pubmed
pubmed-article:3189402pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3189402pubmed:citationSubsetIMlld:pubmed
pubmed-article:3189402pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3189402pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3189402pubmed:statusMEDLINElld:pubmed
pubmed-article:3189402pubmed:monthJullld:pubmed
pubmed-article:3189402pubmed:issn0148-7299lld:pubmed
pubmed-article:3189402pubmed:authorpubmed-author:TaylorK AKAlld:pubmed
pubmed-article:3189402pubmed:authorpubmed-author:de...lld:pubmed
pubmed-article:3189402pubmed:authorpubmed-author:PihK DKDlld:pubmed
pubmed-article:3189402pubmed:authorpubmed-author:LitzC ECElld:pubmed
pubmed-article:3189402pubmed:authorpubmed-author:PescovitzO...lld:pubmed
pubmed-article:3189402pubmed:issnTypePrintlld:pubmed
pubmed-article:3189402pubmed:volume30lld:pubmed
pubmed-article:3189402pubmed:ownerNLMlld:pubmed
pubmed-article:3189402pubmed:authorsCompleteYlld:pubmed
pubmed-article:3189402pubmed:pagination821-33lld:pubmed
pubmed-article:3189402pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:meshHeadingpubmed-meshheading:3189402-...lld:pubmed
pubmed-article:3189402pubmed:year1988lld:pubmed
pubmed-article:3189402pubmed:articleTitleAbsence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome.lld:pubmed
pubmed-article:3189402pubmed:affiliationDepartment of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis.lld:pubmed
pubmed-article:3189402pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3189402pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3189402lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3189402lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3189402lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3189402lld:pubmed