Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and SOS2[original query] |
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| Candidate gene association study of insulin signaling genes and Alzheimer's disease: evidence for SOS2, PCK1, and PPARgamma as susceptibility loci. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Jun 144B (4): 508-16. Hamilton Gillian, Proitsi Petra, Jehu Luke, Morgan Angharad, Williams Julie, O'Donovan Michael C, Owen Michael J, Powell John F, Lovestone Sim |
Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years.
G3 (Bethesda, Md.) 2014 Feb 4 (2): 307-14. Shaffer John R, Polk Deborah E, Wang Xiaojing, Feingold Eleanor, Weeks Daniel E, Lee Myoung-Keun, Cuenco Karen T, Weyant Robert J, Crout Richard J, McNeil Daniel W, Marazita Mary |
| Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications. European journal of human genetics : EJHG 2020 8 29 (1): 51-60. Lissewski Christina, Chune Valérie, Pantaleoni Francesca, De Luca Alessandro, Capri Yline, Brinkmann Julia, Lepri Francesca, Daniele Paola, Leenders Erika, Mazzanti Laura, Scarano Emanuela, Radio Francesca Clementina, Kutsche Kerstin, Kuechler Alma, Gérard Marion, Ranguin Kara, Legendre Marine, Vial Yoann, van der Burgt Ineke, Rinne Tuula, Andreucci Elena, Mastromoro Gioia, Digilio Maria Cristina, Cave Hélène, Tartaglia Marco, Zenker Mart |
| Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing. Frontiers in cardiovascular medicine 2022 2 8 811156. Zhou Yue, Bai Kai, Wang Yu, Meng Zhuo, Zhou Shuang, Jiang Shiwei, Wang Hualin, Wang Jian, Yang Mei, Wang Qingjie, Sun Kun, Chen S |
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