1.
Azevedo CB, Delgado LA, Almeida ML, 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. Int J Contemp Pediatr [Internet]. 2026 Sep. 23 [cited 2026 Sep. 24];13(10):2128-33. Available from: https://www.ijpediatrics.com/index.php/ijcp/article/view/7619