Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
A high proportion of patients with myelodysplasia show characteristic karyotypic abnormalities in bone marrow cells. The most distinctive of the myelodysplastic syndromes is the 5q- syndrome characterized by refractory anemia, poorly lobulated megakaryocytes, and an interstitial deletion of the long...
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| Veröffentlicht in: | Proc Natl Acad Sci U S A |
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| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
National Academy of Sciences
1991
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| Schlagworte: | |
| Online-Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC52045/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1829836/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.88.14.6176 |
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