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...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en: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
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2015
Assuntos:
Case Report
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares