Molecular approaches reveal RUNX1 amplification and a rearrangement of NTRK3, a new leukemia putative gene, in a pediatric case of B-ALL: Discussing the intrachromosomal amplification of chromosome 21 (iAMP21)

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dc.contributor.authorGarcia, Daniela Ribeiro Ney
dc.contributor.authorMatos, Roberto Rodrigues Capela de
dc.contributor.authorOthman, Moneeb A. K.
dc.contributor.authorFerreira, Gerson Moura
dc.contributor.authorSouza, Mariana Tavares de
dc.contributor.authorMonteso, Kelly Cristina de Assis
dc.contributor.authorLand, Marcelo Gerardin Poirot
dc.contributor.authorRibeiro, Raul Corrêa
dc.contributor.authorLiehr, Thomas
dc.contributor.authorSilva, Maria Luiza Macedo
dc.date.accessioned2021-07-13T14:55:55Z
dc.date.available2021-07-13T14:55:55Z
dc.date.issued2018
dc.identifier.urihttp://sr-vmlxaph03:8080/jspui/handle/123456789/3321
dc.publisherINCApt_BR
dc.titleMolecular approaches reveal RUNX1 amplification and a rearrangement of NTRK3, a new leukemia putative gene, in a pediatric case of B-ALL: Discussing the intrachromosomal amplification of chromosome 21 (iAMP21)pt_BR

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