Translocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin

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dc.contributor.authorXochelli, A.
dc.contributor.authorBaliakas, P.
dc.contributor.authorMoore, S.
dc.contributor.authorSole, F.
dc.contributor.authorWickham, N.
dc.contributor.authorSalido, M.
dc.contributor.authorAthanasiadou, A.
dc.contributor.authorOscier, D.
dc.contributor.authorStamatopoulos, K.
dc.date.issued2014
dc.descriptionLetter to the editor
dc.description.statementofresponsibilityAliki Xochelli, Panagiotis Baliakas, Sarah Moore, Francesc Sole, Nicholas Wickham, Marta Salido, Anastasia Athanasiadou, David Oscier and Kostas Stamatopoulos
dc.identifier.citationCancer Genetics, 2014; 207(6):281-283
dc.identifier.doi10.1016/j.cancergen.2014.06.026
dc.identifier.issn2210-7762
dc.identifier.issn2210-7770
dc.identifier.urihttp://hdl.handle.net/2440/93478
dc.language.isoen
dc.publisherElsevier
dc.rights© 2014 Elsevier Inc. All rights reserved.
dc.source.urihttps://doi.org/10.1016/j.cancergen.2014.06.026
dc.titleTranslocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin
dc.typeJournal article
pubs.publication-statusPublished

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