Copy Number Variation
Author:
Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4939-7868-7_14
Reference164 articles.
1. Valsesia A, Mace A, Jacquemont S et al (2013) The growing importance of CNVs: new insights for detection and clinical interpretation. Front Genet 4:92
2. Conrad DF, Pinto D, Redon R et al (2010) Origins and functional impact of copy number variation in the human genome. Nature 464(7289):704–712
3. Feuk L, Carson AR, Scherer SW (2006) Structural variation in the human genome. Nat Rev Genet 7(2):85–97
4. Fiegler H, Redon R, Andrews D et al (2006) Accurate and reliable high-throughput detection of copy number variation in the human genome. Genome Res 16(12):1566–1574
5. Freeman JL, Perry GH, Feuk L et al (2006) Copy number variation: new insights in genome diversity. Genome Res 16(8):949–961
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