Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia

Deletions in the long arm of chromosome 5 or loss of the whole chromosome are rare in childhood Acute Myeloid Leukemia (AML) patients. It is also unknown if the wide variety of breakpoints have diverging implications in the patient’s outcome. Despite -5/5q- abnormalities have usually been described...

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Bibliographic Details
Published in:Mol Cytogenet
Main Authors: de Figueiredo, Amanda Faria, Capela de Matos, Roberto Rodrigues, Othman, Moneeb A. K., Liehr, Thomas, da Costa, Elaine Sobral, Land, Marcelo Geradin Poirot, Ribeiro, Raul C., Abdelhay, Eliana, Silva, Maria Luiza Macedo
Format: Artigo
Language:Inglês
Published: BioMed Central 2015
Subjects:
Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4528810/
https://ncbi.nlm.nih.gov/pubmed/26257826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-015-0167-y
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