JOSHI, A.; JOSHI, J. Recurrent severe hyperbilirubinemia due to compound heterozygous UGT1A1 mutations: an early neonatal presentation of Gilbert syndrome. International Journal of Contemporary Pediatrics, [S. l.], v. 13, n. 2, p. 342–345, 2026. DOI: 10.18203/2349-3291.ijcp20260114. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/7202. Acesso em: 12 feb. 2026.