Targeted Screening and Validation of Copy Number Variations
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-61779-507-7_15
Reference66 articles.
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3. Beckmann,J.S., Sharp,A.J. and Antonarakis,S.E. (2008) CNVs and genetic medicine (excitement and consequences of a rediscovery). Cytogenet.Genome Res., 123, 7–16.
4. Lachman,H.M. (2008) Copy variations in schizophrenia and bipolar disorder. Cytogenet.Genome Res., 123, 27–35.
5. de Smith,A.J., Walters,R.G., Froguel,P. and Blakemore,A.I. (2008) Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease. Cytogenet.Genome Res., 123, 17–26.
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