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Cited by 3,297

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Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors

Kallioniemi, Anne, Kallioniemi, Olli-P., Sudar, Damir, Rutovitz, Denis, Gray, Joe W., Waldman, Fred, Pinkel, Dan·1992·Science

Abstract

Comparative genomic hybridization produces a map of DNA sequence copy number as a function of chromosomal location throughout the entire genome. Differentially labeled test DNA and normal reference DNA are hybridized simultaneously to normal chromosome spreads. The hybridization is detected with two different fluorochromes. Regions of gain or loss of DNA sequences, such as deletions, duplications, or amplifications, are seen as changes in the ratio of the intensities of the two fluorochromes along the target chromosomes. Analysis of tumor cell lines and primary bladder tumors identified 16 different regions of amplification, many in loci not previously known to be amplified.

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Metadata

Authors
Kallioniemi, A., Kallioniemi, O.-P., Sudar, D., Rutovitz, D., Gray, J. W., Waldman, F., & Pinkel, D.
Venue
Science
Published
1992-10-30
Volume
258
Issue
5083
Pages
818-821
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1968046362
Cited by
3,297
References
0
FWCI
28.10
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors. https://app.cochat.ai/papers/10.1126/science.1359641
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Kallioniemi, A., Kallioniemi, O.-P., Sudar, D., Rutovitz, D., Gray, J. W., Waldman, F., & Pinkel, D. (1992). Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors. Science. https://doi.org/10.1126/science.1359641

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