Molecular analysis of exons 8, 9 and 10 of the fibroblast growth factor receptor 2 (FGFR2) gene in two families with index cases of Apert Syndrome. Colombia Medica, [S. l.], v. 46, n. 3, p. 150–153, 2015. DOI: 10.25100/cm.v46i3.1868. Disponível em: https://colombiamedica.univalle.edu.co/index.php/comedica/article/view/1868. Acesso em: 26 dec. 2025.