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Clinical implications of t(11;14)(q13;q32), t(4;14)(p16.3;q32), and -17p13 in myeloma patients treated with high-dose therapy

Fluorescence in situ hybridization (FISH) is more sensitive than conventional cytogenetics for recognizing chromosomal changes. Several FISH-detected abnormalities have been associated with inferior prognosis, including deletion of chromosomes 17 and 13 (Δ13) and t(4;14)(p16.3;q32). We analyzed the...

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Detalhes bibliográficos
Main Authors: Gertz, Morie A., Lacy, Martha Q., Dispenzieri, Angela, Greipp, Philip R., Litzow, Mark R., Henderson, Kimberly J., Van Wier, Scott A., Ahmann, Greg J., Fonseca, Rafael
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2005
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1895302/
https://ncbi.nlm.nih.gov/pubmed/15976175
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2005-04-1411
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