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Article: Concomitant presence of trisomy 21 and del(9q) in acute myeloid leukemia

TitleConcomitant presence of trisomy 21 and del(9q) in acute myeloid leukemia
Authors
Kwong, YLChan, LC
Issue Date1992
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene
Citation
Cancer Genetics And Cytogenetics, 1992, v. 64 n. 1, p. 93-94 How to Cite?
DOI: http://dx.doi.org/10.1016/0165-4608(92)90331-2
AbstractWe report two cases of acute myeloid leukemia with deletion of the long arm of chromosome 9 [del(9q)] and trisomy 21. del(9q) and +21 do not often occur as a sole karyotypic abnormality in acute myeloid leukemia (AML). Their concomitant presence is rare; the significance of the findings in leukemia is discussed.
Persistent Identifierhttp://hdl.handle.net/10722/147940
ISSN
0165-4608
2012 Impact Factor: 1.929
ISI Accession Number ID
WOS:A1992KD81700018

 

DC FieldValueLanguage
dc.contributor.authorKwong, YLen_HK
dc.contributor.authorChan, LCen_HK
dc.date.accessioned2012-05-29T06:10:01Z-
dc.date.available2012-05-29T06:10:01Z-
dc.date.issued1992en_HK
dc.identifier.citationCancer Genetics And Cytogenetics, 1992, v. 64 n. 1, p. 93-94en_HK
dc.identifier.issn0165-4608en_HK
dc.identifier.urihttp://hdl.handle.net/10722/147940-
dc.description.abstractWe report two cases of acute myeloid leukemia with deletion of the long arm of chromosome 9 [del(9q)] and trisomy 21. del(9q) and +21 do not often occur as a sole karyotypic abnormality in acute myeloid leukemia (AML). Their concomitant presence is rare; the significance of the findings in leukemia is discussed.en_HK
dc.languageengen_US
dc.publisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergeneen_HK
dc.relation.ispartofCancer Genetics and Cytogeneticsen_HK
dc.subject.meshAdolescenten_US
dc.subject.meshAdulten_US
dc.subject.meshChromosome Deletionen_US
dc.subject.meshChromosomes, Human, Pair 21en_US
dc.subject.meshChromosomes, Human, Pair 9en_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshKaryotypingen_US
dc.subject.meshLeukemia, Myeloid, Acute - Geneticsen_US
dc.subject.meshMaleen_US
dc.subject.meshTrisomyen_US
dc.titleConcomitant presence of trisomy 21 and del(9q) in acute myeloid leukemiaen_HK
dc.typeArticleen_HK
dc.identifier.emailKwong, YL:ylkwong@hku.hken_HK
dc.identifier.emailChan, LC:chanlc@hkucc.hku.hken_HK
dc.identifier.authorityKwong, YL=rp00358en_HK
dc.identifier.authorityChan, LC=rp00373en_HK
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/0165-4608(92)90331-2en_HK
dc.identifier.pmid1458456-
dc.identifier.scopuseid_2-s2.0-0026948493en_HK
dc.identifier.volume64en_HK
dc.identifier.issue1en_HK
dc.identifier.spage93en_HK
dc.identifier.epage94en_HK
dc.identifier.isiWOS:A1992KD81700018-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridKwong, YL=7102818954en_HK
dc.identifier.scopusauthoridChan, LC=7403540707en_HK
dc.identifier.issnl0165-4608-

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