Skip to main navigation Skip to search Skip to main content

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

  • R. Slater*
  • , E. Smit
  • , W. Kroes
  • , M. Jotterand Bellomo
  • , D. Mühlematter
  • , J. Harbott
  • , H. Behrendt
  • , K. Hählen
  • , A. J. P. Veerman
  • , A. Hagemeijer
  • *Corresponding author for this work
  • University of Amsterdam
  • Erasmus MC
  • University of Lausanne
  • Universitätsklinikum Giessen und Marburg, Standort Giessen
  • Erasmus University Rotterdam
  • Vrije Universiteit Amsterdam

Research output: Contribution to journalReview articleAcademicpeer-review

Abstract

A comparison of cytogenetical data on acute lymphoblastic leukaemia studied at four large European centres has revealed a non-random dicentric chromosome abnormality: dlc(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.
Original languageEnglish
Pages (from-to)1613-1619
JournalLeukemia
Volume9
Issue number10
Publication statusPublished - 1995
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11)'. Together they form a unique fingerprint.

Cite this