Clinical Significance of Previously Cryptic Copy Number Alterations and Loss of Heterozygosity in Pediatric Acute Myeloid Leukemia and Myelodysplastic Syndrome Determined Using Combined Array Comparative Genomic Hybridization plus Single-Nucleotide Polymorphism Microarray Analyses.

This study demonstrates that CGH+SNP microarray can simultaneously detect previously cryptic CNAs and LOH, which may demonstrate prognostic implications. PMID: 25045224 [PubMed - in process]

http://www.ncbi.nlm.nih.gov/pubmed/25045224?dopt=Abstract

Source: J Korean Med Sci - July 1, 2014 Category: Journals (General) Authors: Koh KN, Lee JO, Seo EJ, Lee SW, Suh JK, Im HJ, Seo JJ Tags: J Korean Med Sci Source Type: research