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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/21328
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dc.contributor.authorVendrame-Goloni, C. B.-
dc.contributor.authorVarella-Garcia, M.-
dc.contributor.authorCarvalho-Salles, A. B.-
dc.contributor.authorRuiz, M. A.-
dc.contributor.authorRicci, O.-
dc.contributor.authorFett-Conte, A. C.-
dc.date.accessioned2014-05-20T14:00:18Z-
dc.date.accessioned2016-10-25T17:07:54Z-
dc.date.available2014-05-20T14:00:18Z-
dc.date.available2016-10-25T17:07:54Z-
dc.date.issued2003-02-01-
dc.identifierhttp://dx.doi.org/10.1016/S0165-4608(02)00646-5-
dc.identifier.citationCancer Genetics and Cytogenetics. New York: Elsevier B.V., v. 141, n. 1, p. 71-74, 2003.-
dc.identifier.issn0165-4608-
dc.identifier.urihttp://hdl.handle.net/11449/21328-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/21328-
dc.description.abstractA novel association of t(11;19)(q23;p13) and t(5;16)(q13;q22) was detected by G-banding and spectral karyotyping studies in an 18-year-old patient. While balanced t(11; 19) has been often described in acute myelocytic leukemia (AML) French-American-British Cooperative Group subtypes M4 and M5, this patient was diagnosed with the variant AML-M4 with eosinophilia (AML-M4Eo), which is associated with abnormalities in 16q22 and has good prognosis. However, the patient relapsed after allogeneic transplant and died within 2 years of diagnosis, which suggests that the association of these two translocations correlates with a poor prognosis. This report expands the molecular basis of the variability in clinical outcomes and adds the novel t(5;16)(q13;q22) to the spectrum of chromosome 16q22 abnormalities in AML. (C) 2003 Elsevier B.V. All rights reserved.en
dc.format.extent71-74-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.titleTranslocation (11;19)(q23;p13.3) associated with a novel t(5;16) (ql3;q22) in a patient with acute myelocytic leukemiaen
dc.typeoutro-
dc.contributor.institutionUniv Colorado-
dc.contributor.institutionFUNFARME-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Colorado, Ctr Comprehens Canc, Denver, CO 80202 USA-
dc.description.affiliationFUNFARME, Hemoctr, São Paulo, Brazil-
dc.description.affiliationUniv Hosp, FUNFARME, Bone Marrow Transplant Unit, São Paulo, Brazil-
dc.description.affiliationFAMERP, Sch Med, Dept Mol Biol, São Paulo, Brazil-
dc.description.affiliationUNESP, IBILCE, Dept Biol, São Paulo, Brazil-
dc.description.affiliationUnespUNESP, IBILCE, Dept Biol, São Paulo, Brazil-
dc.identifier.doi10.1016/S0165-4608(02)00646-5-
dc.identifier.wosWOS:000180887400011-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofCancer Genetics and Cytogenetics-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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