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. Colomb Med [Internet]. 2015 Sep. 30 [cited 2025 Dec. 26];46(3):150-3. Available from: https://colombiamedica.univalle.edu.co/index.php/comedica/article/view/1868