SNP Array Karyotyping Allows for the Detection of Uniparental Disomy and Cryptic Chromosomal Abnormalities in MDS/MPD-U and MPD

Author:

Gondek Lukasz P.,Dunbar Andrew J.,Szpurka Hadrian,McDevitt Michael A.,Maciejewski Jaroslaw P.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference39 articles.

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2. Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias.;M Raghavan;Cancer Res.,2005

3. Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays. Nat.Biotechnol.;K Lindblad-Toh,2000

4. Preferential loss of maternal 9p alleles in childhood acute lymphoblastic leukemia.;IM Morison;Blood,2002

5. High-resolution analysis of 9p loss in human cancer cells using single nucleotide polymorphism-based mapping arrays. Cancer Genet.Cytogenet.;J Pei,2006

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