HuGE Literature Finder
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Congenital Heart Diseases: Genetic Risk Variants and Their Methylation Status. Genes 2022 11 13 (11): . Calzada-Dávila Melissa, Calvo-Anguiano Geovana, Martínez-de-Villarreal Laura E, Lugo-Trampe José J, González-Peña Sandra M, Ancer-Rodríguez Patricia R, Hernández-Almaguer María D, Campos-Acevedo Luis |
Relationship between TBX20 gene polymorphism and congenital heart disease. Genetics and molecular research : GMR 2016 Jun 15 (2): . Yang X F, Zhang Y F, Zhao C F, Liu M M, Si J P, Fang Y F, Xing W W, Wang F |
Novel mutations in the transcriptional activator domain of the human TBX20 in patients with atrial septal defect. BioMed research international 2015 2015 718786. Monroy-Muñoz Irma Eloisa, Pérez-Hernández Nonanzit, Rodríguez-Pérez José Manuel, Muñoz-Medina José Esteban, Angeles-Martínez Javier, García-Trejo José J, Morales-Ríos Edgar, Massó Felipe, Sandoval-Jones Juan Pablo, Cervantes-Salazar Jorge, García-Montes José Antonio, Calderón-Colmenero Juan, Vargas-Alarcón Gilber |
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- Page last updated:Mar 20, 2023
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