A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11).
| Data(s) |
1995
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|---|---|
| Resumo |
A comparison of cytogenetical data on acute lymphoblastic leukaemia studied at four large European centres has revealed a non-random dicentric chromosome abnormality: dic(9;20) (p1?3;q11) in 10 patients, nine of whom were children. All had early precursor-B lineage ALL, and eight children had a non-standard risk clinical presentation. The origin of the dicentric chromosome was demonstrated using a range of chromosome banding techniques. This was confirmed by FISH using paints and centromeric probes for chromosomes 9 and 20, together with a number of cosmid probes. The follow-up time of these patients is presently too short and the number of patients too few to determine the prognostic significant of this chromosome abnormality. |
| Identificador |
http://serval.unil.ch/?id=serval:BIB_9F4F7FB32DF1 isbn:0887-6924 pmid:7564498 isiid:A1995TA83500001 |
| Idioma(s) |
en |
| Fonte |
Leukemia, vol. 9, no. 10, pp. 1613-1619 |
| Palavras-Chave | #Adolescent; Child; Child, Preschool; Chromosomes, Human, Pair 20; Chromosomes, Human, Pair 9; Female; Humans; In Situ Hybridization, Fluorescence; Infant; Karyotyping; Male; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma; Precursor Cell Lymphoblastic Leukemia-Lymphoma |
| Tipo |
info:eu-repo/semantics/article article |