Incidental copy-number variants identified by routine genome testing in a clinical population

PURPOSE: Mutational load of susceptibility variants has not been studied on a genomic scale in a clinical population, nor has the potential to identify these mutations as incidental findings during clinical testing been systematically ascertained. METHODS: Array comparative genomic hybridization, a...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Boone, Philip M., Soens, Zachry T., Campbell, Ian M., Stankiewicz, Pawel, Cheung, Sau Wai, Patel, Ankita, Beaudet, Arthur L., Plon, Sharon E., Shaw, Chad A., McGuire, Amy L., Lupski, James R.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2012
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3705759/
https://ncbi.nlm.nih.gov/pubmed/22878507
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2012.95
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