Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes-Reference-Cited by-同舟云学术

Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes

Published:2010-08-19 Issue:11 Volume:49 Page:1014-1023
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

Barresi Vincenza,Romano Alessandra,Musso Nicolò,Capizzi Carmela,Consoli Carla,Martelli Maria Paola,Palumbo Giuseppe,Di Raimondo Francesco,Condorelli Daniele F.

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference43 articles.

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2. Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis;Bullinger;Leukemia,2010

3. Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia;Dicker;Blood,2007

4. Trisomy 13: A new recurring chromosome abnormality in acute leukemia;Döhner;Blood,1990

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