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Detection of trisomy 12 by fluorescent in situ hybridization (FISH) in chronic lymphocytic leukemia Genet. Mol. Biol.
Chauffaille,Maria de Lourdes L.F.; Marques,Eliana Azevedo; Oliveira,Jose Salvador Rodrigues de; Rodrigues,Maria Madalena; Figueiredo,Maria Stella; Romeo,Maura; Yamamoto,Mihoko; Kerbauy,José.
Chronic lymphocytic leukemia (CLL) presents a varying incidence of karyotypic abnormalities whose detection is complicated by difficulties in obtaining mitosis for analysis in this type of mature lymphocyte disorder. Since the introduction of molecular cytogenetics (FISH = fluorescent in situ hybridization), applying centromeric probes for chromosome 12 has made it possible to detect a higher percentage of trisomy 12 cases. The objective of the present study was to detect trisomy 12 by FISH (alpha satellite probe) in 13 patients with CLL whose karyotypes by G-banding were either normal or inadequate. Using this method trisomy 12 was detected in three patients in a percentage of positive cells varying from 55.5% to 79%, showing that FISH is a sensitive and...
Tipo: Info:eu-repo/semantics/article
Ano: 2000 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572000000300005
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