The translocation t119q23p13 TCF3PBX1 fusion is the most common recurrent genetic abnormality detected amongst patients with Bcell lymphoblastic leukaemia in Johannesburg South Africa

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dc.citation.doi10.4102/SAJO.V5I0.179
dc.citation.epage6
dc.citation.spage1
dc.contributor.authorJenifer Vaughan
dc.contributor.authorNikki Bouwer
dc.contributor.authorPascale Willem
dc.contributor.authorTracey Wiggill
dc.contributor.authorKatherine Hodkinson
dc.date.accessioned2023-04-13T14:09:18Z
dc.date.available2023-04-13T14:09:18Z
dc.identifier.citationDOAJ
dc.identifier.issn2518-8704
dc.identifier.urihttps://hdl.handle.net/10539/35144
dc.journal.titleSOUTH AFRICAN JOURNAL OF ONCOLOGY
dc.journal.volume5
dc.titleThe translocation t119q23p13 TCF3PBX1 fusion is the most common recurrent genetic abnormality detected amongst patients with Bcell lymphoblastic leukaemia in Johannesburg South Africa
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