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A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome
BACKGROUND: Children with Down syndrome (DS) have an enhanced risk of developing acute leukemia, with the most common subtype being acute megakaryoblastic leukemia (AMKL). Myeloid leukemia in Down syndrome (ML-DS) is considered a disease with distinct clinical and biological features. There are few...
Sparad:
| I publikationen: | Mol Cytogenet |
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| Huvudupphovsmän: | , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2017
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5594429/ https://ncbi.nlm.nih.gov/pubmed/28912835 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-017-0335-3 |
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