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)...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Eur J Haematol
Main Authors: 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.
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2018
Teme:
Original Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7379948/
https://ncbi.nlm.nih.gov/pubmed/30270457
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ejh.13179
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki