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Cancer Genet Cytogenet ; 161(1): 82-5, 2005 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16080963

RESUMO

We present a case of del(14)(q21) as a sole abnormality in a 4-year-old boy diagnosed with precursor B-cell acute lymphoblastic leukemia (pre-B ALL). To our knowledge, this is the first case of isolated del(14)(q21) in pre-B ALL. Two pretreatment bone marrow samples obtained 5 days apart were analyzed by cytogenetics. The G-banded karyotypes of the two samples were similar, differing only in the ratio of normal/abnormal metaphases detected. Both samples showed a del(14)(q21) as the only abnormality. Fluorescence in situ hybridization performed using the probes TEL/AML1 and immunoglobulin heavy chain (IGH) showed no fusion involving the TEL and AML1 genes and only a single IGH signal in 20% of the interphase cells analyzed.


Assuntos
Cromossomos Humanos Par 4/genética , Deleção de Genes , Proteínas de Fusão Oncogênica/genética , Leucemia-Linfoma Linfoblástico de Células Precursoras B/genética , Pré-Escolar , Subunidade alfa 2 de Fator de Ligação ao Core , Rearranjo Gênico , Humanos , Cadeias Pesadas de Imunoglobulinas , Hibridização in Situ Fluorescente , Interfase , Cariotipagem , Masculino
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