pubmed-article:3052797 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:3052797 | lifeskim:mentions | umls-concept:C0023467 | lld:lifeskim |
pubmed-article:3052797 | lifeskim:mentions | umls-concept:C0026986 | lld:lifeskim |
pubmed-article:3052797 | lifeskim:mentions | umls-concept:C0009013 | lld:lifeskim |
pubmed-article:3052797 | lifeskim:mentions | umls-concept:C1533148 | lld:lifeskim |
pubmed-article:3052797 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:3052797 | pubmed:dateCreated | 1988-12-6 | lld:pubmed |
pubmed-article:3052797 | pubmed:abstractText | Different and unrelated chromosome changes were found to occur in a patient with a myelodysplastic syndrome with rapid evolution to acute nonlymphocytic leukemia. A 6p anomaly was found during the chronic phase and a del(9q) characterized the cells in the leukemic phase. Deletions with a breakpoint in 9q31 appeared to be associated with more aggressive disease. | lld:pubmed |
pubmed-article:3052797 | pubmed:language | eng | lld:pubmed |
pubmed-article:3052797 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3052797 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:3052797 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3052797 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:3052797 | pubmed:month | Oct | lld:pubmed |
pubmed-article:3052797 | pubmed:issn | 0165-4608 | lld:pubmed |
pubmed-article:3052797 | pubmed:author | pubmed-author:Van den... | lld:pubmed |
pubmed-article:3052797 | pubmed:author | pubmed-author:GrossiAA | lld:pubmed |
pubmed-article:3052797 | pubmed:author | pubmed-author:MecucciCC | lld:pubmed |
pubmed-article:3052797 | pubmed:author | pubmed-author:FerriniP RPR | lld:pubmed |
pubmed-article:3052797 | pubmed:author | pubmed-author:BernabeiP APA | lld:pubmed |
pubmed-article:3052797 | pubmed:author | pubmed-author:RingressiAA | lld:pubmed |
pubmed-article:3052797 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:3052797 | pubmed:day | 15 | lld:pubmed |
pubmed-article:3052797 | pubmed:volume | 35 | lld:pubmed |
pubmed-article:3052797 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:3052797 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:3052797 | pubmed:pagination | 213-21 | lld:pubmed |
pubmed-article:3052797 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
pubmed-article:3052797 | pubmed:meshHeading | pubmed-meshheading:3052797-... | lld:pubmed |
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pubmed-article:3052797 | pubmed:meshHeading | pubmed-meshheading:3052797-... | lld:pubmed |
pubmed-article:3052797 | pubmed:year | 1988 | lld:pubmed |
pubmed-article:3052797 | pubmed:articleTitle | 6p+ and 9q- in two chromosomally distinct clones occurring in a case of myelodysplastic syndrome evolving to acute nonlymphocytic leukemia. | lld:pubmed |
pubmed-article:3052797 | pubmed:affiliation | Department of Hematology, University of Florence, Italy. | lld:pubmed |
pubmed-article:3052797 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:3052797 | pubmed:publicationType | Review | lld:pubmed |
pubmed-article:3052797 | pubmed:publicationType | Case Reports | lld:pubmed |
pubmed-article:3052797 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |