Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia

OBJECTIVE: Acute myeloid leukemia (AML) can be subtyped based on recurrent cytogenetic and molecular genetic abnormalities with diagnostic and prognostic significance. Although cytogenetic characterization classically involves conventional chromosome and/or fluorescence in situ hybridization (FISH)...

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Detalles Bibliográficos
Autores principales: Aypar, Umut, Smoley, Stephanie A., Pitel, Beth A., Pearce, Kathryn E., Zenka, Roman M., Vasmatzis, George, Johnson, Sarah H., Smadbeck, James B., Peterson, Jess F., Geiersbach, Katherine B., Van Dyke, Daniel L., Thorland, Erik C., Jenkins, Robert B., Ketterling, Rhett P., Greipp, Patricia T., Kearney, Hutton M., Hoppman, Nicole L., Baughn, Linda B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379948/
https://www.ncbi.nlm.nih.gov/pubmed/30270457
http://dx.doi.org/10.1111/ejh.13179

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379948/
https://www.ncbi.nlm.nih.gov/pubmed/30270457
http://dx.doi.org/10.1111/ejh.13179

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