Whole Exome Association of Rare Deletions in Multiplex Oral Cleft Families

By sequencing the exomes of distantly related individuals in multiplex families, rare mutational and structural changes to coding DNA can be characterized and their relationship to disease risk can be assessed. Recently, several rare single nucleotide variants (SNVs) were associated with an increase...

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Detalhes bibliográficos
Publicado no:Genet Epidemiol
Main Authors: Fu, Jack, Beaty, Terri H., Scott, Alan F., Hetmanski, Jacqueline, Parker, Margaret M., Wilson, Joan E. Bailey, Marazita, Mary L., Mangold, Elisabeth, Albacha-Hejazi, Hasan, Murray, Jeffrey C., Bureau, Alexandre, Carey, Jacob, Cristiano, Stephen, Ruczinski, Ingo, Scharpf, Robert B.
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5154821/
https://ncbi.nlm.nih.gov/pubmed/27910131
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.22010
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