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Article: Deletion of Xq23 is a recurrent karyotypic abnormality in acute myeloid leukemia

TitleDeletion of Xq23 is a recurrent karyotypic abnormality in acute myeloid leukemia
Authors
Issue Date2000
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene
Citation
Cancer Genetics And Cytogenetics, 2000, v. 122 n. 1, p. 33-36 How to Cite?
AbstractDeletion of chromosome Xq23 has been reported in a number of solid tumors, including soft tissue sarcoma, malignant melanoma, astrocytoma, and adenocarcinoma. The deleted Xq often occurs in a setting of very complex karyotypic changes. A similar abnormality has also been described in rare cases of acute myeloid leukemia (AML) but in no other hematologic malignancies. In this study, we report the occurrence of del(X)(q23) in two cases of AML. Copyright (C) 2000 Elsevier Science Inc.
Persistent Identifierhttp://hdl.handle.net/10722/148210
ISSN
2012 Impact Factor: 1.929
2013 SCImago Journal Rankings: 0.872
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorWong, KFen_US
dc.contributor.authorSiu, LLPen_US
dc.contributor.authorSo, CCen_US
dc.date.accessioned2012-05-29T06:11:31Z-
dc.date.available2012-05-29T06:11:31Z-
dc.date.issued2000en_US
dc.identifier.citationCancer Genetics And Cytogenetics, 2000, v. 122 n. 1, p. 33-36en_US
dc.identifier.issn0165-4608en_US
dc.identifier.urihttp://hdl.handle.net/10722/148210-
dc.description.abstractDeletion of chromosome Xq23 has been reported in a number of solid tumors, including soft tissue sarcoma, malignant melanoma, astrocytoma, and adenocarcinoma. The deleted Xq often occurs in a setting of very complex karyotypic changes. A similar abnormality has also been described in rare cases of acute myeloid leukemia (AML) but in no other hematologic malignancies. In this study, we report the occurrence of del(X)(q23) in two cases of AML. Copyright (C) 2000 Elsevier Science Inc.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.meshAcute Diseaseen_US
dc.subject.meshChromosome Deletionen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshIn Situ Hybridization, Fluorescenceen_US
dc.subject.meshKaryotypingen_US
dc.subject.meshLeukemia, Myeloid - Geneticsen_US
dc.subject.meshMiddle Ageden_US
dc.subject.meshX Chromosomeen_US
dc.titleDeletion of Xq23 is a recurrent karyotypic abnormality in acute myeloid leukemiaen_US
dc.typeArticleen_US
dc.identifier.emailSo, CC:scc@pathology.hku.hken_US
dc.identifier.authoritySo, CC=rp00391en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/S0165-4608(00)00271-5en_US
dc.identifier.pmid11104030-
dc.identifier.scopuseid_2-s2.0-0034305149en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0034305149&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume122en_US
dc.identifier.issue1en_US
dc.identifier.spage33en_US
dc.identifier.epage36en_US
dc.identifier.isiWOS:000165287100007-
dc.publisher.placeUnited Statesen_US

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