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A Genotype-First Approach to Defining the Subtypes of a Complex Disease

Medical genetics typically entails the detailed characterization of a patient’s phenotypes followed by genotyping to discover the responsible gene or mutation. Here, we propose that the systematic discovery of genetic variants associated with complex diseases such as autism are progressing to a poin...

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Detalhes bibliográficos
Main Authors: Stessman, Holly A., Bernier, Raphael, Eichler, Evan E.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4076166/
https://ncbi.nlm.nih.gov/pubmed/24581488
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2014.02.002
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