t(1;3)(p36.3;q21.1)

Preferred Label : t(1;3)(p36.3;q21.1);

NCIt definition : A chromosomal translocation involving breakpoints within the p36.3 band on the short arm of chromosome 1 and the q21.1 band on the long arm of chromosome 3. This rearrangement is rare and may be associated with myeloproliferative disorders.;

Détails

Origin ID

C217183;

cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 3 [NCIt concept]

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