Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and TBX3[original query] |
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Genetic analysis of the TBX3 gene promoter in ventricular septal defects. Gene 2013 Jan 512 (2): 185-8. Chen Dongfeng, Qiao Yanli, Meng Haihong, Pang Shuchao, Huang Wenhui, Zhang Hongyu, Yan |
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. Cardiovascular research 2015 Jun 106 (3): 520-9. Behr Elijah R, Savio-Galimberti Eleonora, Barc Julien, Holst Anders G, Petropoulou Evmorfia, Prins Bram P, Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A, Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J, Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M, Bezzina Connie R, Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia, , Jamshidi Yal |
Association of T-box gene polymorphisms with the risk of Wolff-Parkinson-White syndrome in a Han Chinese population. Medicine 2022 Aug 101 (32): e30046. Han Bing, Wang Yongxiang, Zhao Jing, Lan Qingsu, Zhang Jin, Meng Xiaoxue, Jin Jianjian, Bai Ming, Zhang Zhe |
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- Page last updated:Mar 25, 2024
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