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An unusual case of high hyperdiploid childhood ALL with cryptic BCR/ABL1 rearrangement
BACKGROUND: Both high hyperdiploidy (HeH) and the translocation t(9;22)(q34;q11) are recurrent abnormalities in childhood B-cell acute lymphoblastic leukemia (ALL) and both are used in current classification to define different genetic and prognostic subtypes of the disease. The coexistence of these...
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| Autors principals: | , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4213530/ https://ncbi.nlm.nih.gov/pubmed/25360156 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-014-0072-9 |
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