HuGE Literature Finder
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| Comparison of DNA methylation patterns across tissue types in infants with tetralogy of Fallot. Birth defects research 2022 9 114 (17): 1101-1111. Nelson Jennifer S, Kwok Cheuk, Braganca Nicholas E, Lopez Daralys L, Espina Rey Andrea P, Robinson Matthew, Ebert Steven |
| Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children. Molecular genetics & genomic medicine 2019 Mar e612. Behiry Eman G, Al-Azzouny Mahmoud A, Sabry Dina, Behairy Ola G, Salem Nessrine |
| Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease. Journal of human genetics 2015 Oct . Yoshida Akiko, Morisaki Hiroko, Nakaji Mai, Kitano Masataka, Kim Ki-Sung, Sagawa Koichi, Ishikawa Shiro, Satokata Ichiro, Mitani Yoshihide, Kato Hitoshi, Hamaoka Kenji, Echigo Shigeyuki, Shiraishi Isao, Morisaki Takayu |
| Identification of Copy Number Variations in Isolated Tetralogy of Fallot. Pediatric cardiology 2015 Jun . Aguayo-Gómez Adolfo, Arteaga-Vázquez Jazmín, Svyryd Yevgeniya, Calderón-Colmenero Juan, Zamora-González Carlos, Vargas-Alarcón Gilberto, Mutchinick Osvaldo |
| Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot. American journal of medical genetics. Part A 2014 Dec 164A (12): 3100-7. Baban Anwar, Postma Alex Vincent, Marini Monica, Trocchio Gianluca, Santilli Antonella, Pelegrini Monica, Sirleto Pietro, Lerone Margherita, Albanese Sonia Bernadette, Barnett Phil, Boogerd Cornelis Job, Dallapiccola Bruno, Digilio Maria Cristina, Ravazzolo Roberto, Pongiglione Giaco |
| Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot. Journal of translational medicine 2014 2 12 31. Sheng Wei, Qian Yanyan, Zhang Ping, Wu Yao, Wang Huijun, Ma Xiaojing, Chen Long, Ma Duan, Huang Guoyi |
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