Health / Medical Topics |
T(3;5)(q25;q34)
A cytogenetic abnormality that refers to the translocation of the long arm (q25) of chromosome 3 and the long arm (q34) of chromosome 5. It is associated with the development of acute myeloid leukemia arising from myelodysplastic syndrome, acute myeloid leukemia with multilineage dysplasia, and acute myeloid leukemia with myelodysplasia-related changes. (NCI Thesaurus)
YOU MAY ALSO LIKE
A chromosomal translocation associated with Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor and Olfactory Neuroblastoma.
A chromosomal translocation associated with creation of a fusion between the PML and RARA genes. It is seen in variants of Acuteā¦
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.
t(12;21) is a chromosomal translocation, involved in TEL-AML1 oncogene formation, that produces a chimeric gene encoding a protein consisting of the N-terminalā¦