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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Bibliographische Detailangaben
Veröffentlicht in:Mol Cytogenet
Hauptverfasser: 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
Sprache:Inglês
Veröffentlicht: BioMed Central 2015
Schlagworte:
Case Report
Online Zugang: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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