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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Detalles Bibliográficos
Autores principales: Tüfekçi, Özlem, Ören, Hale, Yenigürbüz, Fatma Demir, Gözmen, Salih, Karapınar, Tuba Hilkay, İrken, Gülersu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451488/
https://www.ncbi.nlm.nih.gov/pubmed/26316488
http://dx.doi.org/10.4274/tjh.2014.0034

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451488/
https://www.ncbi.nlm.nih.gov/pubmed/26316488
http://dx.doi.org/10.4274/tjh.2014.0034

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