HASSAN, M.; YASMEEN, B. H. N.; KHAN, M.; MUKTI, A. Apert Syndrome: A Rare Genetic Disorder. Northern International Medical College Journal, [S. l.], v. 11, n. 2, p. 475–477, 2021. DOI: 10.3329/nimcj.v11i2.54066. Disponível em: https://banglajol.info/index.php/NIMCJ/article/view/54066. Acesso em: 10 aug. 2022.