Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/13921
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dc.contributor.authorRodrigues, Eliane Ferreira-
dc.contributor.authorSouza, Daiane Corrêa de Souza e-
dc.contributor.authorCamargo, Adriana-
dc.contributor.authorTavares, Rita de Cássia Barbosa da Silva-
dc.contributor.authorBouzas, Luis Fernando da Silva-
dc.contributor.authorSouza, Maria Helena Ornellas de-
dc.contributor.authorFernandez, Teresa de Souza-
dc.date.accessioned2023-05-24T19:01:02Z-
dc.date.available2023-05-24T19:01:02Z-
dc.date.issued2007-10-
dc.identifier.issn1873-4456-
dc.identifier.urihttps://ninho.inca.gov.br/jspui/handle/123456789/13921-
dc.description.abstractA 13-year-old boy with hypocellular primary myelodysplastic syndrome, classified as refractory cytopenia, underwent umbilical cord blood transplantation. Cytogenetic analysis revealed two rare biclonal chromosomal aberrations, del(17)(p12) and del(11)(q23). Cytogenetic analysis was a valu able tool in diagnosis, in clinical decision-making, and in treatment and follow-up. To our knowl edge, this is the first reported case of cytogenetic biclonality involving chromosomes 17 and 11.pt_BR
dc.subjectCitogenéticapt_BR
dc.subjectCytogeneticspt_BR
dc.subjectSíndromes Mielodisplásicaspt_BR
dc.subjectMyelodysplastic Syndromespt_BR
dc.subjectTransplantept_BR
dc.subjectTransplantationpt_BR
dc.subjectchildpt_BR
dc.subjectCriançapt_BR
dc.subjectAberrações Cromossômicaspt_BR
dc.subjectChromosome Aberrationspt_BR
dc.titleCytogenetic biclonality in a child with hypocellular primary myelodysplastic syndromept_BR
dc.TypeArticlept_BR
Appears in Collections:Hospital do Câncer I (HCI)



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