" /> t(10;19)(q26;q13) - CISMeF





Preferred Label : t(10;19)(q26;q13);

NCIt definition : A cytogenetic abnormality that refers to the translocation involving the genes CIC (capicua transcriptional suppressor) on chromosome 19 and DUX4L (double homeobox 4-like) on chromosome 10 resulting in CIC-DUX4L fusion.;

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14/05/2024


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