Clinical Utility of Array Comparative Genomic Hybridization for Detection of Chromosomal Abnormalities in Pediatric Acute Lymphoblastic Leukemia

BACKGROUND: Accurate detection of recurrent chromosomal abnormalities is critical to assign patients to risk-based therapeutic regimens for pediatric acute lymphoblastic leukemia (ALL). PROCEDURE: We investigated the utility of array comparative genomic hybridization (aCGH) for detection of chromoso...

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Detalhes bibliográficos
Main Authors: Rabin, Karen R., Man, Tsz-Kwong, Yu, Alexander, Folsom, Matthew R., Zhao, Yi-Jue, Rao, Pulivarthi H., Plon, Sharon E., Naeem, Rizwan C.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4063297/
https://ncbi.nlm.nih.gov/pubmed/18253961
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pbc.21488
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