| Literature DB >> 11520571 |
W Emberger1, A Behmel, M Tschernigg, H L Seewann, E Petek, P M Kroisel, K Wagner.
Abstract
We report a 59-year-old, male, chronic myeloid leukemia patient with a rare variant Philadelphia (Ph) translocation t(9;10;22)(q34;q22;q11). Fluorescence in situ hybridization with whole chromosome paints was used to confirm the cytogenetic findings. With a BCR/ABL-specific probe, the known rearrangement on the derivative chromosome 22 was found. The prognostic implications as well as the relevance of the additional breakpoint region 10q22 are discussed.Entities:
Mesh:
Year: 2001 PMID: 11520571 DOI: 10.1016/s0165-4608(01)00417-4
Source DB: PubMed Journal: Cancer Genet Cytogenet ISSN: 0165-4608