1) Inazawa J, Inoue J, Imoto I. Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes. 2004. Cancer Sci 95: 559-563.

2) Feuk L, Carson AR, Scherer SW. Structural variation in the human genome. 2006. Nat Rev Genet. 7:85-97.

3) Iafrate AJ, Feuk L, Rivera MN et al. Detection of large-scale variation in the human genome. Nat Genet. 2004. 36: 949-51.

4) Sebat J, Lakshmi B, Troge J et al. Large-scale copy number polymorphism in the human genome. Science. 2004. 305: 525-8.

5) Lee C, Iafrate AJ, Brothman AR. Copy number variations and clinical cytogenetic diagnosis of constitutional disorders. Nat Genet. 2007. 39: S48–54.

6) Redon R, Ishikawa S, Fitch KR et al. Global variation in copy number in the human genome. Nature. 2006. 444: 444-454.

7) 稲澤譲治、蒔田芳男、羽田明：アレイCGH診断活用ガイドブック．医薬ジャーナル社、東京、2008，p18-p24

8) Hayashi S, Honda S, Minaguchi M et al. Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis. J Hum Genet. 2007. 52: 397-405.

9) LaFramboise T. Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances. Nucleic Acids Res. 2009. 37: 4181-93.

10) Stankiewicz P, Lupski JR. Structural variation in the human genome and its role in disease. Annu Rev Med. 2010. 61:437-55.