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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Primary Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525270/
https://www.ncbi.nlm.nih.gov/pubmed/16004724
http://dx.doi.org/10.1186/1479-7364-2-2-81

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525270/
https://www.ncbi.nlm.nih.gov/pubmed/16004724
http://dx.doi.org/10.1186/1479-7364-2-2-81

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