A carregar...

The ‘Common Disease-Common Variant’ Hypothesis and Familial Risks

The recent large genotyping studies have identified a new repertoire of disease susceptibility loci of unknown function, characterized by high allele frequencies and low relative risks, lending support to the common disease-common variant (CDCV) hypothesis. The variants explain a much larger proport...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Hemminki, Kari, Försti, Asta, Bermejo, Justo Lorenzo
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2423486/
https://ncbi.nlm.nih.gov/pubmed/18560565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0002504
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!