A Comprehensive Analysis of Common Copy-Number Variations in the Human Genome

Segmental copy-number variations (CNVs) in the human genome are associated with developmental disorders and susceptibility to diseases. More importantly, CNVs may represent a major genetic component of our phenotypic diversity. In this study, using a whole-genome array comparative genomic hybridizat...

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Main Authors: Wong, Kendy K. , deLeeuw, Ronald J. , Dosanjh, Nirpjit S. , Kimm, Lindsey R. , Cheng, Ze , Horsman, Douglas E. , MacAulay, Calum , Ng, Raymond T. , Brown, Carolyn J. , Eichler, Evan E. , Lam, Wan L. 
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Human Genetics 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1785303/
https://ncbi.nlm.nih.gov/pubmed/17160897
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