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dc.contributor.authorCabezas, María
dc.contributor.authorCamos, Mireia
dc.contributor.authorRives, Susana
dc.contributor.authorGarcía-Orad Carles, África ORCID
dc.contributor.authorLópez López, Elixabet ORCID
dc.contributor.authorDapena, Josep L.
dc.contributor.authorCaballín, María R.
dc.contributor.authorArmengol, Gemma
dc.date.accessioned2024-04-30T17:26:21Z
dc.date.available2024-04-30T17:26:21Z
dc.date.issued2018-05-29
dc.identifier.citationBritish Journal of Haematology 185(1) :159-162 (2019)es_ES
dc.identifier.issn0007-1048
dc.identifier.issn1365-2141
dc.identifier.urihttp://hdl.handle.net/10810/66966
dc.description.abstractDespite intensification of therapy, 20% of children with acute lymphoblastic leukaemia (ALL) relapse (Ceppi et al, 2015). The different response to chemotherapy may be partially explained by inherited genetic variants, e.g. single nucleotide polymorphisms (SNPs) and copy number variants (CNVs). However, clinically useful genetic predictors of ALL treatment response are yet to be identified.es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.titleImpact of polymorphisms in apoptosis-related genes on the outcome of childhood acute lymphoblastic leukaemiaes_ES
dc.typeinfo:eu-repo/semantics/otheres_ES
dc.rights.holder© 2018 British Society for Haematology and John Wiley & Sons Ltdes_ES
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/full/10.1111/bjh.15415es_ES
dc.identifier.doi10.1111/bjh.15415
dc.departamentoesGenética, antropología física y fisiología animales_ES
dc.departamentoeuGenetika,antropologia fisikoa eta animalien fisiologiaes_ES


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