SOHAIL, A. S.; KRISHNAMURTHY, V.; SANIKAM, H.; KARIYAPPA, P.; RAO, U. S. Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings. International Journal of Contemporary Pediatrics, [S. l.], v. 7, n. 12, p. 2387–2390, 2020. DOI: 10.18203/2349-3291.ijcp20205102. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/3697. Acesso em: 6 nov. 2025.