Joshi, Anjali, and Jeetinder Joshi. “Recurrent Severe Hyperbilirubinemia Due to Compound Heterozygous UGT1A1 Mutations: An Early Neonatal Presentation of Gilbert Syndrome”. International Journal of Contemporary Pediatrics 13, no. 2 (January 27, 2026): 342–345. Accessed February 12, 2026. https://www.ijpediatrics.com/index.php/ijcp/article/view/7202.