| Health / Medical Topics |
T(15;17)(q22;q12)
A chromosomal translocation associated with creation of a fusion between the PML and RARA genes. It is seen in variants of Acute Promyelocytic Leukemia. (NCI Thesaurus)
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A cytogenetic finding indicating that the translocation (14;18) is present in cells.
A cytogenetic finding indicating that the translocation (14;18) is not present in cells.
A chromosomal translocation that involves the chromosomes 14 and 16.
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