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High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9. 2006 (English)In: Genes Chromosomes Cancer, ISSN 1045-2257, Vol. 45, no 8, p. 731-9Article in journal (Refereed) Published

Place, publisher, year, edition, pages

2006. Vol. 45, no 8, p. 731-9

Keywords [en]

Acute Disease, Child; Preschool, Chromosome Breakage, Chromosomes; Human; Pair 12, Chromosomes; Human; Pair 7, Cohort Studies, Female, Homeodomain Proteins/*genetics/metabolism, Humans, In Situ Hybridization; Fluorescence, Infant, Infant; Newborn, Leukemia; Lymphocytic; Acute/*genetics, Leukemia; Myeloid/*genetics, Male, Models; Genetic, Oncogene Proteins; Fusion/genetics, Proto-Oncogene Proteins c-ets/genetics, Repressor Proteins/genetics, Research Support; Non-U.S. Gov't, Transcription Factors/*genetics/metabolism, Translocation; Genetic

Identifiers

URN: urn:nbn:se:uu:diva-21274PubMedID: 16646086OAI: oai:DiVA.org:uu-21274DiVA, id: diva2:49047

Available from: 2006-12-18 Created: 2006-12-18 Last updated: 2011-01-11

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PubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16646086&dopt=Citation

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Lönnerholm, Gudmar

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Department of Women's and Children's Health

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