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Successful treatment and integrated genomic analysis of an infant with FIP1L1-RARA fusion–associated myeloid neoplasm
FIP1L1-RARA–a ssociated neoplasm is a very rare and aggressive disease, with only 3 previously reported cases in the literature. Here, we describe a 9-month-old boy who presented with a FIP1L1-RARA fusion–associated myelodysplastic/myeloproliferative neoplasm-like overlap syndrome, with similarities...
Autores principales: | Miltiadous, Oriana, Petrova-Drus, Kseniya, Kaicker, Shipra, Mathew, Susan, Kluk, Michael, Geyer, Julia T., Rodriguez-Sanchez, Irene, Bouvier, Nancy, Inghirami, Giorgio, Stieglitz, Elliot, Khedoudja, Nafa, Benayed, Ryma, Richardson, Michelle, Anderson, Wade, Benhamida, Jamal, You, Daoqi, Londono, Dory, Kung, Andrew L., Prockop, Susan E., Roshal, Mikhail, Zhang, Yanming, Shukla, Neerav |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Hematology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864666/ https://www.ncbi.nlm.nih.gov/pubmed/34551074 http://dx.doi.org/10.1182/bloodadvances.2021004966 |
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