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A novel translocation t(1;7)(p36;q34) in three patients with acute myeloid leukaemia

✍ Scribed by G. Specchia; A. Cuneo; V. Liso; R. Contino; D. Pastore; E. Gentile; M. Rocchi; G. L. Castoldi

Book ID
108672206
Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
177 KB
Volume
105
Category
Article
ISSN
0007-1048

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## Abstract The t(1;21)(p36;q22) is a recurrent chromosome abnormality associated with therapy‐related acute myeloid leukemia (AML). Although involvement of __RUNX1__ has been detected by fluorescence in situ hybridization analysis, the partner gene has not been reported previously. We identified a