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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/65224
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dc.contributor.authorCavalli, L. R.-
dc.contributor.authorCavaliéri, L. M B-
dc.contributor.authorRibeiro, L. A.-
dc.contributor.authorCavalli, I. J.-
dc.contributor.authorSilveira, R.-
dc.contributor.authorRogatto, Silvia Regina-
dc.date.accessioned2014-05-27T11:18:17Z-
dc.date.accessioned2016-10-25T18:14:40Z-
dc.date.available2014-05-27T11:18:17Z-
dc.date.available2016-10-25T18:14:40Z-
dc.date.issued1997-11-03-
dc.identifierhttp://dx.doi.org/10.1111/j.1601-5223.1997.00261.x-
dc.identifier.citationHereditas, v. 126, n. 3, p. 261-268, 1997.-
dc.identifier.issn0018-0661-
dc.identifier.urihttp://hdl.handle.net/11449/65224-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/65224-
dc.description.abstractChromosome analysis was performed on samples from 20 Brazilian patients with breast cancer. All the samples were from untreated patients who presented the clinical symptoms for months or years before surgical intervention. Six cases showed axillary lymph node metastases. Clonal chromosome abnormalities were detected in all cases. The numerical alterations most frequently observed involved the loss of chromosomes X, 19, 20, and 22 followed by gain of chromosomes 9 and 8. Among the structural anomalies observed, there was preferential involvement of chromosomes 11, 6, 1, 7, 3, and 12, supporting previous reports that these chromosomes may harbour genes of importance in the development of breast tumors. Two cases with a family history of breast cancer had in common total or partial trisomy 1.en
dc.format.extent261-268-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectaxillary lymph node-
dc.subjectbrazil-
dc.subjectbreast cancer-
dc.subjectchromosome 1-
dc.subjectchromosome 11-
dc.subjectchromosome 12-
dc.subjectchromosome 19-
dc.subjectchromosome 20-
dc.subjectchromosome 22-
dc.subjectchromosome 3-
dc.subjectchromosome 6-
dc.subjectchromosome 7-
dc.subjectchromosome 8-
dc.subjectchromosome 9-
dc.subjectclinical article-
dc.subjectcytogenetics-
dc.subjectfemale-
dc.subjecthuman-
dc.subjectlymph node metastasis-
dc.subjectmale-
dc.subjectnumerical chromosome aberration-
dc.subjectpartial trisomy-
dc.subjectstructural chromosome aberration-
dc.subjectX chromosome-
dc.subjectAdult-
dc.subjectAged-
dc.subjectAged, 80 and over-
dc.subjectBrazil-
dc.subjectBreast Neoplasms-
dc.subjectBreast Neoplasms, Male-
dc.subjectCarcinoma, Ductal, Breast-
dc.subjectChromosome Aberrations-
dc.subjectChromosome Disorders-
dc.subjectChromosome Mapping-
dc.subjectChromosomes, Human-
dc.subjectFemale-
dc.subjectHumans-
dc.subjectKaryotyping-
dc.subjectLymphatic Metastasis-
dc.subjectMale-
dc.subjectMiddle Aged-
dc.subjectNeoplasms-
dc.subjectTrisomy-
dc.subjectX Chromosome-
dc.titleCytogenetic evaluation of 20 primary breast carcinomasen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal do Paraná (UFPR)-
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionHospital Nossa Senhora Das Gracas-
dc.description.affiliationDepartment of Genetics Univ. Federal do Paraná, Curitiba, PR-
dc.description.affiliationDepartment of Biology CCB Universidade Estadual de Londrina, Londrina, PR-
dc.description.affiliationDepartment of Genetics Instituto de Biociências UNESP, Botucatu, SP-
dc.description.affiliationOncology Service Hosp. Nossa Senhora Das Gracas, Curitiba, PR-
dc.description.affiliationDepartamento de Genética IB UNESP, Botucatu - Sao Paulo CEP 18607-070-
dc.description.affiliationUnespDepartment of Genetics Instituto de Biociências UNESP, Botucatu, SP-
dc.description.affiliationUnespDepartamento de Genética IB UNESP, Botucatu - Sao Paulo CEP 18607-070-
dc.identifier.doi10.1111/j.1601-5223.1997.00261.x-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-0030656520.pdf-
dc.relation.ispartofHereditas-
dc.identifier.scopus2-s2.0-0030656520-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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