AZEVEDO, C. B.; DELGADO, L. A.; ALMEIDA, M. L.; RODRIGUES, S.; ALMEIDA, A. A novel pathogenic heterozygous mutation in the CDC42BPB gene: a case report of global developmental delay potentially associated with Chilton-Okur-Chung syndrome. International Journal of Contemporary Pediatrics, [S. l.], v. 13, n. 10, p. 2128–2133, 2026. DOI: 10.18203/2349-3291.ijcp20263321. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/7619. Acesso em: 24 sep. 2026.