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pubmed-article:3094418pubmed:abstractTextWe have followed one patient with Philadelphia (Ph)-negative chronic myelogenous leukemia and identified an additional four patients from the literature who showed the rearrangement in the breakpoint cluster region (bcr) on chromosome 22 characteristic of Ph-positive chronic myelogenous leukemia. The clinical course of these five patients was similar to that of Ph-positive patients, with easily controlled leukocyte counts, a prolonged benign phase, and prolonged survival. Furthermore, we have shown, for the first time, that bcr rearrangement in Ph-negative chronic myelogenous leukemia can result in expression of the aberrant 210-kilodalton bcr-abl fusion protein, which has been strongly implicated in Ph-positive leukemogenesis. Research data pertaining to possible cytogenetic mechanisms leading to production of p210bcr-abl in the absence of the Ph chromosome are reviewed. Molecular analysis provides an important tool for classifying and predicting prognosis of some patients with Ph-negative chronic myelogenous leukemia.lld:pubmed
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pubmed-article:3094418pubmed:dateRevised2009-11-19lld:pubmed
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pubmed-article:3094418pubmed:year1986lld:pubmed
pubmed-article:3094418pubmed:articleTitleRearrangement in the breakpoint cluster region and the clinical course in Philadelphia-negative chronic myelogenous leukemia.lld:pubmed
pubmed-article:3094418pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3094418pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:3094418pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed