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Chromosome aberrations including der(6)t(2;6)(p15;p21.3) and der(22)t(3;22)(p21;p11) in the evolution of essential thrombocythemia to myelofibrosis with myeloid metaplasia.
Umeå University, Faculty of Medicine, Public Health and Clinical Medicine, Medicine.
Umeå University, Faculty of Medicine, Public Health and Clinical Medicine, Medicine.
2006 (English)In: Cancer Genet Cytogenet, ISSN 0165-4608, Vol. 165, no 1, 87-9 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2006. Vol. 165, no 1, 87-9 p.
Keyword [en]
Aged, Chromosome Aberrations, Chromosome Mapping, Chromosomes; Human; Pair 2, Chromosomes; Human; Pair 22, Chromosomes; Human; Pair 3, Chromosomes; Human; Pair 6, Disease Progression, Female, Humans, Myelofibrosis/*genetics, Myeloid Metaplasia/*genetics, Prognosis, Thrombocytosis/complications/*genetics
Identifiers
URN: urn:nbn:se:umu:diva-15358DOI: doi:10.1016/j.cancergencyto.2005.11.010PubMedID: 16490605OAI: oai:DiVA.org:umu-15358DiVA: diva2:155030
Available from: 2007-07-04 Created: 2007-07-04 Last updated: 2011-01-11Bibliographically approved

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Publisher's full textPubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16490605&dopt=Citation

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