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Management of Two Juvenile Myelomonocytic Leukemia Patients According to Clinical and Genetic Features
Juvenile myelomonocytic leukemia (JMML) is a rare clonal myeloproliferative disorder of childhood. Major progress has been achieved in diagnosis and the understanding of the pathogenesis of JMML by identifying the genetic pathologies that occur in patients. Mutations of RAS, NF1, PTPN11, and CBL are...
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| Pubblicato in: | Turk J Haematol |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Galenos Publishing
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4451488/ https://ncbi.nlm.nih.gov/pubmed/26316488 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/tjh.2014.0034 |
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