Azevedo, C. B., Delgado, L. A., Almeida, M. L., Rodrigues, S., & Almeida, A. (2026). 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, 13(10), 2128–2133. https://doi.org/10.18203/2349-3291.ijcp20263321