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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Stessman, Holly A., Bernier, Raphael, Eichler, Evan E.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2014
Gaiak:
Sarrera elektronikoa: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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