" /> t(6;9)(q22-23;p23-24) - CISMeF





Preferred Label : t(6;9)(q22-23;p23-24);

NCIt definition : A cytogenetic abnormality that refers to the translocation of the long arm (q22-23) of chromosome 6 and the short arm (p23-24) of chromosome 9. It results in the formation of MYB/NFIB fusion gene.;

NCI Metathesaurus CUI : CL1920671;

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08/05/2025


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