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Article: A novel t(7;17)(q11;q11) as the sole karyotypic abnormality in childhood pre-B-cell acute lymphoblastic leukemia [1]

TitleA novel t(7;17)(q11;q11) as the sole karyotypic abnormality in childhood pre-B-cell acute lymphoblastic leukemia [1]
Authors
Issue Date1998
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene
Citation
Cancer Genetics And Cytogenetics, 1998, v. 104 n. 1, p. 70-71 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/148129
ISSN
2012 Impact Factor: 1.929
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLee, ACWen_US
dc.contributor.authorMa, SKen_US
dc.contributor.authorWan, TSKen_US
dc.contributor.authorChing, LMen_US
dc.contributor.authorChan, LCen_US
dc.date.accessioned2012-05-29T06:11:01Z-
dc.date.available2012-05-29T06:11:01Z-
dc.date.issued1998en_US
dc.identifier.citationCancer Genetics And Cytogenetics, 1998, v. 104 n. 1, p. 70-71en_US
dc.identifier.issn0165-4608en_US
dc.identifier.urihttp://hdl.handle.net/10722/148129-
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.meshChilden_US
dc.subject.meshChromosome Aberrations - Geneticsen_US
dc.subject.meshChromosome Disordersen_US
dc.subject.meshChromosomes, Human, Pair 17 - Geneticsen_US
dc.subject.meshChromosomes, Human, Pair 7 - Geneticsen_US
dc.subject.meshHumansen_US
dc.subject.meshKaryotypingen_US
dc.subject.meshMaleen_US
dc.subject.meshPrecursor B-Cell Lymphoblastic Leukemia-Lymphoma - Geneticsen_US
dc.subject.meshPrecursor Cell Lymphoblastic Leukemia-Lymphoma - Geneticsen_US
dc.subject.meshTranslocation, Genetic - Geneticsen_US
dc.titleA novel t(7;17)(q11;q11) as the sole karyotypic abnormality in childhood pre-B-cell acute lymphoblastic leukemia [1]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(97)00393-2en_US
dc.identifier.pmid9648563-
dc.identifier.scopuseid_2-s2.0-0032125706en_US
dc.identifier.hkuros41698-
dc.identifier.volume104en_US
dc.identifier.issue1en_US
dc.identifier.spage70en_US
dc.identifier.epage71en_US
dc.identifier.isiWOS:000074334500012-
dc.publisher.placeUnited Statesen_US
dc.identifier.issnl0165-4608-

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