Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variation

Understanding the distribution of human genetic variation is an important foundation for research into the genetics of common diseases. Some of the alleles that modify common disease risk are themselves likely to be common and, thus, amenable to identification using gene-association methods. A probl...

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Detalhes bibliográficos
Main Authors: Shriver, Mark D, Mei, Rui, Parra, Esteban J, Sonpar, Vibhor, Halder, Indrani, Tishkoff, Sarah A, Schurr, Theodore G, Zhadanov, Sergev I, Osipova, Ludmila P, Brutsaert, Tom D, Friedlaender, Jonathan, Jorde, Lynn B, Watkins, W Scott, Bamshad, Michael J, Gutierrez, Gerardo, Loi, Halina, Matsuzaki, Hajime, Kittles, Rick A, Argyropoulos, George, Fernandez, Jose R, Akey, Joshua M, Jones, Keith W
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2005
Assuntos:
Primary Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3525270/
https://ncbi.nlm.nih.gov/pubmed/16004724
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-7364-2-2-81
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