A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11).


Autoria(s): Slater R.; Smit E.; Kroes W.; Bellomo M.J.; Mühlematter D.; Harbott J.; Behrendt H.; Hählen K.; Veerman A.J.; Hagemeijer A.
Data(s)

1995

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