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Article: Deletion 9q as the sole karyotypic abnormality in myelocytic disorders: A new case of myelodysplastic syndrome and its prognostic implications in acute myelocytic leukemia [2]

TitleDeletion 9q as the sole karyotypic abnormality in myelocytic disorders: A new case of myelodysplastic syndrome and its prognostic implications in acute myelocytic leukemia [2]
Authors
Issue Date2003
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene
Citation
Cancer Genetics And Cytogenetics, 2003, v. 145 n. 2, p. 184-186 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/148348
ISSN
2012 Impact Factor: 1.929
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorWan, TSKen_US
dc.contributor.authorMa, ESKen_US
dc.contributor.authorLam, CCKen_US
dc.contributor.authorChan, LCen_US
dc.contributor.authorLee, KKen_US
dc.contributor.authorAu, WYen_US
dc.date.accessioned2012-05-29T06:12:23Z-
dc.date.available2012-05-29T06:12:23Z-
dc.date.issued2003en_US
dc.identifier.citationCancer Genetics And Cytogenetics, 2003, v. 145 n. 2, p. 184-186en_US
dc.identifier.issn0165-4608en_US
dc.identifier.urihttp://hdl.handle.net/10722/148348-
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.meshAgeden_US
dc.subject.meshChromosome Deletionen_US
dc.subject.meshChromosomes, Human, Pair 9en_US
dc.subject.meshHumansen_US
dc.subject.meshKaryotypingen_US
dc.subject.meshLeukemia, Myeloid - Geneticsen_US
dc.subject.meshLeukemia, Myeloid, Acute - Diagnosis - Geneticsen_US
dc.subject.meshMaleen_US
dc.subject.meshMyelodysplastic Syndromes - Geneticsen_US
dc.subject.meshPrognosisen_US
dc.titleDeletion 9q as the sole karyotypic abnormality in myelocytic disorders: A new case of myelodysplastic syndrome and its prognostic implications in acute myelocytic leukemia [2]en_US
dc.typeArticleen_US
dc.identifier.emailChan, LC:chanlc@hkucc.hku.hken_US
dc.identifier.authorityChan, LC=rp00373en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/S0165-4608(03)00060-8en_US
dc.identifier.pmid12935935-
dc.identifier.scopuseid_2-s2.0-0041662166en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0041662166&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume145en_US
dc.identifier.issue2en_US
dc.identifier.spage184en_US
dc.identifier.epage186en_US
dc.identifier.isiWOS:000185059700017-
dc.publisher.placeUnited Statesen_US
dc.identifier.issnl0165-4608-

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