1. Ahn YS, Lee JW, Bang JK, Lee DB. Three Cases of Apert Syndrome (Acrocephalosyndactyly). J Korean Pediatr Soc 1994;37:1149-1155.
2. Ibrahimi OA, Chiu ES, McCarthy JG, Mohammadi M. Understanding the molecular basis of Apert syndrome. Plast Reconstr Surg 2005;115:264-270.
3. Rare mutations ofFGFR2causing apert syndrome: identification of the first partial gene deletion, and anAluelement insertion from a new subfamily
4. Kwon MK, Yun JY, Kim MR, Lee KH, Lee HR, Kim KN. A Case of Apert's Syndrome with Encephalocele and Hypogenesis of Corpus Callosum. J Korean Pediatr Soc 2001;44:832-836.
5. Soancă A, Dudea D, Gocan H, Roman A, Culic B. Oral manifestations in Apert syndrome: case presentation and a brief review of the literature. Rom J Morphol Embryol 2010;51:581-584.