A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridization

BACKGROUND: Nonrandom clonal chromosomal aberrations can be detected in approximately 55% of adult patients with acute myeloid leukemia (AML). Recurrent cytogenetic abnormalities play an important role in diagnosis, classification and prognosis of AML. However, several chromosomal abnormalities have...

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Detalles Bibliográficos
Autor principal: Kjeldsen, Eigil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180307/
https://www.ncbi.nlm.nih.gov/pubmed/25279000
http://dx.doi.org/10.1186/s13039-014-0063-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180307/
https://www.ncbi.nlm.nih.gov/pubmed/25279000
http://dx.doi.org/10.1186/s13039-014-0063-x

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