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De novo acute myeloid leukemia with t(8;21)(q22;q22) and monosomy 7

The t(8: 21)(q22;q22) is the most common cytogenetic abnormality, usually with a favorable risk, in acute myeloid leukemia (AML). This translocation is not only of diagnostic significance but also has impact on survival outcomes and therapeutic implications. However, patients with adverse outcome in...

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Detalhes bibliográficos
Main Authors: Harish Kumar, Paresh Singhal, Ajay Malik, Sanjeevan Sharma
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer Medknow Publications 2019-01-01
Colecção:Journal of Applied Hematology
Assuntos:
Acesso em linha:http://www.jahjournal.org/article.asp?issn=1658-5127;year=2019;volume=10;issue=3;spage=99;epage=102;aulast=Kumar
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