Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/2745
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dc.contributor.authorMatos, Roberto Rodrigues Capela de-
dc.contributor.authorOthman, Moneeb A. K.-
dc.contributor.authorFerreira, Gerson Moura-
dc.contributor.authorMonteso, Kelly Cristina de Assis-
dc.contributor.authorSouza, Mariana Tavares de-
dc.contributor.authorRouxinol, Soraia-
dc.contributor.authorMelo, Joana-
dc.contributor.authorCarreira, Isabel Maria Marques-
dc.contributor.authorLiehr, Thomas-
dc.contributor.authorSilva, Maria Luiza Macedo-
dc.date.accessioned2021-07-03T00:22:51Z-
dc.date.available2021-07-03T00:22:51Z-
dc.date.issued2019-
dc.identifier.urihttp://sr-vmlxaph03:8080/jspui/handle/123456789/2745-
dc.publisherINCApt_BR
dc.titleCytogenomic studies highlight a novel putative gene and somatic homozygous loss of SH2B3 gene and its presence in constitutive cells: discussing iAMP21 leukemogenic mechanisms in pediatric acute lymphoblastic leukemiapt_BR
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