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2. 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. Koh KN; Lee JO; Seo EJ; Lee SW; Suh JK; Im HJ; Seo JJ J Korean Med Sci; 2014 Jul; 29(7):926-33. PubMed ID: 25045224 [TBL] [Abstract][Full Text] [Related]
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7. Importance of using comparative genomic hybridization to improve detection of chromosomal changes in childhood acute lymphoblastic leukemia. Jarosová M; Holzerová M; Jedlicková K; Mihál V; Zuna J; Starý J; Pospísilová D; Zemanová Z; Trka J; Blazek J; Pikalová Z; Indrák K Cancer Genet Cytogenet; 2000 Dec; 123(2):114-22. PubMed ID: 11156736 [TBL] [Abstract][Full Text] [Related]
8. Integration of cytogenomic data for furthering the characterization of pediatric B-cell acute lymphoblastic leukemia: a multi-institution, multi-platform microarray study. Baughn LB; Biegel JA; South ST; Smolarek TA; Volkert S; Carroll AJ; Heerema NA; Rabin KR; Zweidler-McKay PA; Loh M; Hirsch B Cancer Genet; 2015; 208(1-2):1-18. PubMed ID: 25678190 [TBL] [Abstract][Full Text] [Related]
9. Structural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute lymphoblastic leukemia. Kowalczyk JR; Babicz M; Gaworczyk A; Lejman M; Winnicka D; Styka B; Jaszczuk I Cancer Genet Cytogenet; 2010 Jul; 200(2):161-6. PubMed ID: 20620600 [TBL] [Abstract][Full Text] [Related]
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