| Literature DB >> 2768519 |
E V Davison1, A D Pearson, J Emslie, M M Reid, A Malcolm, A W Craft.
Abstract
A child with disseminated Ewing's sarcoma underwent cytogenetic investigations which showed different structural rearrangements of chromosome 22 at diagnosis (?ring22), and at relapse [t(10;22)], but the classic translocation t(11;22) was not detectable. This case provides further evidence of the importance of chromosome 22 in this disease, while raising some questions about the central importance of the translocation between chromosomes 11 and 22.Entities:
Mesh:
Year: 1989 PMID: 2768519 PMCID: PMC1142053 DOI: 10.1136/jcp.42.8.797
Source DB: PubMed Journal: J Clin Pathol ISSN: 0021-9746 Impact factor: 3.411