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Detection of submicroscopic chromosomal deletions in aniridia patients using fluorescence in situ hybridization and a panel of cosmids covering the WT1 gene

*Corresponding author for this work
  • University College London
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

A series of cosmids have been isolated from a human chromosome 11-specific cosmid library using the human Wilms tumour predisposition gene cDNA, WT33. Seven overlapping cosmids were isolated which cover the genomic sequence of WT1 and in situ hybridisation shows that they all localise to the p13 region of chromosome 11. Chromosomes from patients with aniridia and Wilms tumour, and a small subband deletion in 11p13, were analysed and no hybridisation signal was seen on the deletion chromosomes. These cosmids, therefore, can be used to analyse chromosomes from patients with sporadic aniridia for submicroscopic deletions. Aniridia patients who show normal hybridisation patterns on both chromosomes need no longer be screened for Wilms tumours.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 937-940 (4 pages)

Journal (Volume, Issue Number)

International journal of oncology (Volume 3, Issue 5)

Publication milestones

  • Published - 1993

Publication status

Published - 1993

ISSN

1019-6439

Publication IDs

  • Scopus: 0027360810

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