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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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| Udgivet i: | Eur J Haematol |
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| Main Authors: | , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
John Wiley and Sons Inc.
2018
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| Fag: | |
| Online adgang: | 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 |
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