Accurate Detection of Uniparental Disomy and Microdeletions by SNP Array Analysis in Myelodysplastic Syndromes with Normal Cytogenetics

Progress in the management of patients with myelodysplastic syndromes (MDS) has been hampered by the inability to detect cytogenetic abnormalities in 40-60% of cases. We prospectively analyzed matched pairs of bone marrow and buccal cell (normal) DNA samples from 51 MDS patients by single nucleotide...

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Detalles Bibliográficos
Autores principales: Heinrichs, Stefan, Kulkarni, Rima V., Bueso-Ramos, Carlos E., Levine, Ross L., Loh, Mignon L., Li, Cheng, Neuberg, Donna, Kornblau, Steven M., Issa, Jean-Pierre, Gilliland, D. Gary, Garcia-Manero, Guillermo, Kantarjian, Hagop M., Estey, Elihu H., Look, A. Thomas
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950785/
https://www.ncbi.nlm.nih.gov/pubmed/19387468
http://dx.doi.org/10.1038/leu.2009.82

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