Common variants in the GDF5-BFZB region are associated with variation in human height

Identifying genetic variants that influence human height will further our understanding of skeletal growth and development. A number of rare genetic variants have been convincingly and reproducibly associated with height in Mendelian syndromes, and common variants in HMGA2 were recently found to be...

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Detalhes bibliográficos
Main Authors: Sanna, Serena, Jackson, Anne U., Nagaraja, Ramaiah, Willer, Cristen J., Chen, Wei-Min, Bonnycastle, Lori L., Shen, Haiqing, Timpson, Nicholas, Lettre, Guillaume, Usala, Gianluca, Chines, Peter S., Stringham, Heather M., Dei, Mariano, Lai, Sandra, Albai, Giuseppe, Crisponi, Laura, Naitza, Silvia, Doheny, Kimberly F., Pugh, Elizabeth W., Ben-Shlomo, Yoav, Ebrahim, Shah, Lawlor, Debbie A., Bergman, Richard N., Watanabe, Richard M., Uda, Manuela, Tuomilehto, Jaakko, Coresh, Josef, Hirschhorn, Joel N., Shuldiner, Alan R., Schlessinger, David, Collins, Francis S., Smith, George Davey, Boerwinkle, Eric, Cao, Antonio, Boehnke, Michael, Abecasis, Gonçalo R., Mohlke, Karen L.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2914680/
https://ncbi.nlm.nih.gov/pubmed/18193045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.74
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