Ве молиме користете го овој идентификатор да го цитирате или поврзете овој запис: http://hdl.handle.net/20.500.12188/11554
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dc.contributor.authorOhyashiki, Ken_US
dc.contributor.authorKocova, Men_US
dc.contributor.authorOhyashiki, J Hen_US
dc.contributor.authorRyan, D Hen_US
dc.contributor.authorRowe, J Men_US
dc.contributor.authorSandberg, A Aen_US
dc.date.accessioned2021-03-25T11:04:53Z-
dc.date.available2021-03-25T11:04:53Z-
dc.date.issued1986-03-01-
dc.identifier.issn0165-4608-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/11554-
dc.description.abstractA case of a non-T, non-B acute lymphoblastic leukemia with a translocation between chromosomes #1 and #9 is described. The breakpoints in these chromosomes were determined to be at bands 1q23 and 9p22, respectively. The breakpoint in chromosome #1 was at the same site as that in a subgroup of acute lymphoblastic leukemia with t(1;19), and the breakpoint in #9 was the same as that in t(9;11)(p22;q23) in acute monoblastic leukemia. We discuss the possible association between these chromosome bands (1q23, 9p22, 11q23, and 19p13) and the morphologic features of the leukemic cells. The breakpoint in chromosome band 1q23 may be specifically associated with acute lymphoblastic leukemia.en_US
dc.language.isoenen_US
dc.publisherELSEVIER SCIENCE INCen_US
dc.relation.ispartofCancer genetics and cytogeneticsen_US
dc.titleTranslocation between chromosomes 1 and 9 in childhood acute lymphoblastic leukemiaen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/0165-4608(86)90196-2-
dc.identifier.volume21-
dc.identifier.issue1-
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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