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Article: A novel t(2;3)(q31;p13) in acute myelocytic leukemia

TitleA novel t(2;3)(q31;p13) in acute myelocytic leukemia
Authors
Wong, KFSo, C
Issue Date2002
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene
Citation
Cancer Genetics And Cytogenetics, 2002, v. 138 n. 1, p. 77-79 How to Cite?
DOI: http://dx.doi.org/10.1016/S0165-4608(02)00576-9
AbstractWe report a case of acute myelocytic leukemia without maturation exhibiting a novel t(2;3)(q31;p13). Conventional cytogenetics showed the concomitant occurrence of a single metaphase with 47,XX,+8. Nevertheless, interphase cytogenetics by fluorescence in situ hybridization using a chromosome 8 α-satellite DNA probe showed that the percentage of cells with three hybridization signals was within the control range. © 2002 Elsevier Science Inc. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/148299
ISSN
0165-4608
2012 Impact Factor: 1.929
ISI Accession Number ID
WOS:000178558300014
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorWong, KFen_US
dc.contributor.authorSo, Cen_US
dc.date.accessioned2012-05-29T06:12:05Z-
dc.date.available2012-05-29T06:12:05Z-
dc.date.issued2002en_US
dc.identifier.citationCancer Genetics And Cytogenetics, 2002, v. 138 n. 1, p. 77-79en_US
dc.identifier.issn0165-4608en_US
dc.identifier.urihttp://hdl.handle.net/10722/148299-
dc.description.abstractWe report a case of acute myelocytic leukemia without maturation exhibiting a novel t(2;3)(q31;p13). Conventional cytogenetics showed the concomitant occurrence of a single metaphase with 47,XX,+8. Nevertheless, interphase cytogenetics by fluorescence in situ hybridization using a chromosome 8 α-satellite DNA probe showed that the percentage of cells with three hybridization signals was within the control range. © 2002 Elsevier Science Inc. All rights reserved.en_US
dc.languageengen_US
dc.publisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergeneen_US
dc.relation.ispartofCancer Genetics and Cytogeneticsen_US
dc.subject.meshChromosomes, Human, Pair 2 - Geneticsen_US
dc.subject.meshChromosomes, Human, Pair 3 - Geneticsen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshKaryotypingen_US
dc.subject.meshLeukemia, Myeloid, Acute - Geneticsen_US
dc.subject.meshMiddle Ageden_US
dc.subject.meshTranslocation, Genetic - Geneticsen_US
dc.titleA novel t(2;3)(q31;p13) in acute myelocytic leukemiaen_US
dc.typeArticleen_US
dc.identifier.emailSo, C:scc@pathology.hku.hken_US
dc.identifier.authoritySo, C=rp00391en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/S0165-4608(02)00576-9en_US
dc.identifier.pmid12419590-
dc.identifier.scopuseid_2-s2.0-0036805489en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0036805489&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume138en_US
dc.identifier.issue1en_US
dc.identifier.spage77en_US
dc.identifier.epage79en_US
dc.identifier.isiWOS:000178558300014-
dc.publisher.placeUnited Statesen_US
dc.identifier.issnl0165-4608-

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