The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia

Recurrent chromosomal abnormalities and gene mutations detected at the time of diagnosis of acute myeloid leukemia (AML) are associated with particular disease features, treatment response and survival of AML patients, and are used to denote specific disease entities in the World Health Organization...

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Detalles Bibliográficos
Autores principales: Eisfeld, A-K, Mrózek, K, Kohlschmidt, J, Nicolet, D, Orwick, S, Walker, C J, Kroll, K W, Blachly, J S, Carroll, A J, Kolitz, J E, Powell, B L, Wang, E S, Stone, R M, de la Chapelle, A, Byrd, J C, Bloomfield, C D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628133/
https://www.ncbi.nlm.nih.gov/pubmed/28321123
http://dx.doi.org/10.1038/leu.2017.86

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628133/
https://www.ncbi.nlm.nih.gov/pubmed/28321123
http://dx.doi.org/10.1038/leu.2017.86

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