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Cancer Genet Cytogenet ; 138(2): 149-52, 2002 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-12505261

RESUMO

A 32-year-old man was newly diagnosed with acute myelocytic leukemia, classified as acute myeloblastic leukemia with maturation (AML-M2) according to the French-American-British classification system. Conventional chromosome analysis before chemotherapy treatment revealed an abnormal karyotype: a possible segmental duplication of 11q23, plus a translocation between chromosomes 15 and 17 [t(15;17) (q22;q21.1)] in the majority of cells analyzed. Fluorescence in situ hybridization analysis using commercially available probes confirmed the cytogenetic findings. To our knowledge, this is the first report of a combination of t(15;17) and a segmental duplication of 11q23 in a patient with AML-M2.


Assuntos
Cromossomos Humanos Par 11/genética , Cromossomos Humanos Par 15/genética , Cromossomos Humanos Par 17/genética , Duplicação Gênica , Leucemia Mieloide Aguda/genética , Translocação Genética/genética , Adulto , Medula Óssea/patologia , Humanos , Hibridização in Situ Fluorescente , Masculino
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