High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

Author:

Pinkel Daniel,Segraves Richard,Sudar Damir,Clark Steven,Poole Ian,Kowbel David,Collins Colin,Kuo Wen-Lin,Chen Chira,Zhai Ye,Dairkee Shanaz H.,Ljung Britt-marie,Gray Joe W.,Albertson Donna G.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference31 articles.

1. Kallioniemi, A. et al. Comparative genomic hybridization for cytogenetic analysis of solid tumors. Science 258, 818–821 (1992).

2. Tanner, M.M. et al. Increased copy number at 20q13 in breast cancer: defining the critical region and exclusion of candidate genes. Cancer Res. 54, 4257–4260 (1994).

3. Tanner, M.M. et al. Independent amplification and frequent co-amplification of three nonsyntenic regions on the long arm of chromosome 20 in human breast cancer. Cancer Res. 56, 3441–3445 (1996).

4. Bärlund, M. et al. Increased copy number at 17q22-q24 by CGH in breast cancer is due to high-level amplification of two separate regions. Genes Chromosomes Cancer 20, 372–376 (1997).

5. Ning, Y. et al. A complete set of human telomeric probes and their clinical application. Nature Genet. 14, 86–89 (1996).

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