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

Identifying genetic variants that influence human height will advance our understanding of skeletal growth and development. Several rare genetic variants have been convincingly and reproducibly associated with height in mendelian syndromes, and common variants in the transcription factor gene HMGA2...

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Veröffentlicht in:Nature genetics Jg. 40; H. 2; S. 198 - 203
Hauptverfasser: 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, Scott, Laura J, 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
Format: Journal Article
Sprache:Englisch
Veröffentlicht: New York Nature Publishing Group US 01.02.2008
Nature Publishing Group
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ISSN:1061-4036, 1546-1718, 1546-1718
Online-Zugang:Volltext
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