## Abstract In acute myeloid leukemia (AML), nonrandom clonal chromosome aberrations are detectable in βΌ55% of adult cases. Translocation t(8;21)(q22;q22) resulting in the 5β²__RUNX1__/3β²__RUNX1T1__ fusion gene occurs in βΌ8% of AML cases. Also, ins(8;21) and ins(21;8) have been described that show a
Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22)
β Scribed by Bowen, P. ;Fitzgerald, P. H. ;Gardner, R. J. M. ;Biederman, B. ;Veale, A. M. O.
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 611 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0148-7299
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