“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, vol. 46, no. 3, Sept. 2015, pp. 150-3, https://doi.org/10.25100/cm.v46i3.1868.