Volume 106, Issue 1 pp. 111-114

Two-colour FISH detection of the inv(16) in interphase nuclei of patients with acute myeloid leukaemia

Hans G. Dauwerse

Hans G. Dauwerse

Department of Human Genetics, Leiden University Medical Centre, Leiden

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Elizabeth M. E. Smit

Elizabeth M. E. Smit

Department of Cell Biology and Genetics, Erasmus University, Rotterdam

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Rachel H. Giles

Rachel H. Giles

Department of Human Genetics, Leiden University Medical Centre, Leiden

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Rosalyn Slater

Rosalyn Slater

Department of Cell Biology and Genetics, Erasmus University, Rotterdam

Department of Clinical Genetics, Erasmus University, Rotterdam, The Netherlands

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Martijn H. Breuning

Martijn H. Breuning

Department of Human Genetics, Leiden University Medical Centre, Leiden

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Anne Hagemeijer

Anne Hagemeijer

Department of Cell Biology and Genetics, Erasmus University, Rotterdam

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Bert A. Van Der Reijden

Bert A. Van Der Reijden

Department of Human Genetics, Leiden University Medical Centre, Leiden

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First published: 25 December 2001
Citations: 7
Dr Dauwerse Department of Human Genetics, Leiden University Medical Centre, Wassenaarseweg 72, 2333AL Leiden, The Netherlands. e-mail: [email protected]

Abstract

The inv(16)(p13q22) and t(16;16)(p13;q22) in acute myeloid leukaemia are associated with a relatively good prognosis but are difficult to detect using classic cytogenetics. We have designed a two-colour fluorescence in situ hybridization approach that uses two DNA probes that map close to and on either side of the inv(16) p-arm breakpoint region. This new strategy clearly detected the inv(16)(p13q22)/t(16;16)(p13;q22) on both metaphase chromosomes and in interphase nuclei, even when they are of poor quality. This procedure also detected the inv(16) in cases with an additional deletion of sequences proximal to the 16p-arm breakpoint which is present in 20% of all cases.

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