pubmed-article:3189402 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:3189402 | lifeskim:mentions | umls-concept:C0041432 | lld:lifeskim |
pubmed-article:3189402 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
pubmed-article:3189402 | lifeskim:mentions | umls-concept:C0004903 | lld:lifeskim |
pubmed-article:3189402 | lifeskim:mentions | umls-concept:C0332197 | lld:lifeskim |
pubmed-article:3189402 | lifeskim:mentions | umls-concept:C0262496 | lld:lifeskim |
pubmed-article:3189402 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:3189402 | pubmed:dateCreated | 1988-12-7 | lld:pubmed |
pubmed-article:3189402 | pubmed:abstractText | Monozygotic 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:3189402 | pubmed:language | eng | lld:pubmed |
pubmed-article:3189402 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3189402 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:3189402 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3189402 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3189402 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:3189402 | pubmed:month | Jul | lld:pubmed |
pubmed-article:3189402 | pubmed:issn | 0148-7299 | lld:pubmed |
pubmed-article:3189402 | pubmed:author | pubmed-author:TaylorK AKA | lld:pubmed |
pubmed-article:3189402 | pubmed:author | pubmed-author:de... | lld:pubmed |
pubmed-article:3189402 | pubmed:author | pubmed-author:PihK DKD | lld:pubmed |
pubmed-article:3189402 | pubmed:author | pubmed-author:LitzC ECE | lld:pubmed |
pubmed-article:3189402 | pubmed:author | pubmed-author:PescovitzO... | lld:pubmed |
pubmed-article:3189402 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:3189402 | pubmed:volume | 30 | lld:pubmed |
pubmed-article:3189402 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:3189402 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:3189402 | pubmed:pagination | 821-33 | lld:pubmed |
pubmed-article:3189402 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:3189402 | pubmed:meshHeading | pubmed-meshheading:3189402-... | lld:pubmed |
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pubmed-article:3189402 | pubmed:meshHeading | pubmed-meshheading:3189402-... | lld:pubmed |
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pubmed-article:3189402 | pubmed:meshHeading | pubmed-meshheading:3189402-... | lld:pubmed |
pubmed-article:3189402 | pubmed:year | 1988 | lld:pubmed |
pubmed-article:3189402 | pubmed:articleTitle | Absence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome. | lld:pubmed |
pubmed-article:3189402 | pubmed:affiliation | Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis. | lld:pubmed |
pubmed-article:3189402 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:3189402 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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