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Identification and characterisation of constitutional chromosome abnormalities using arrays of bacterial artificial chromosomes

  • J. K. Cowell(corresponding author)
    ,
  • Y. D. Wang
    ,
  • K. Head
    ,
  • J. Conroy
    ,
  • D. McQuaid
    ,
  • N. J. Nowak
*Corresponding author for this work
  • Roswell Park Cancer Institute
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

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

Abstract

Constitutional chromosome deletions and duplications frequently predispose to the development of a wide variety of cancers. We have developed a microarray of 6000 bacterial artificial chromosomes for array-based comparative genomic hybridisation, which provides an average resolution of 750 kb across the human genome. Using these arrays, subtle gains and losses of chromosome regions can be detected in constitutional cells, following a single overnight hybridisation. In this report, we demonstrate the efficiency of this procedure in identifying constitutional deletions and duplications associated with predisposition to retinoblastoma, Wilms tumour and Beckwith-Wiedemann syndrome. copy; 2004 Cancer Research UK.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 860-865 (6 pages)

Journal (Volume, Issue Number)

British Journal of Cancer (Volume 90, Issue 4)

Publication milestones

  • Published - 02/23/2004

Publication status

Published - 02/23/2004

ISSN

0007-0920

Publication IDs

  • Scopus: 1642267572
  • PubMed: 14970865

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
1.42
SciVal
Author count
6
SciVal
citations
33
SciVal
Paper percentile
79
Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
5
Citation count
34

Funding Details

We would like to thank Dr Robin Winter (Institute of Child Health, University of London) for help in assessing the clinical phenotypes. This work was supported in part by the Roswell Park Cancer Institute’s NCI Cancer Center Support Grant, CA 16056.
FundersFunding number
NCI
P30CA016056
RPCI
-