Joshi, A., and J. Joshi. “Recurrent Severe Hyperbilirubinemia Due to Compound Heterozygous UGT1A1 Mutations: An Early Neonatal Presentation of Gilbert Syndrome”. International Journal of Contemporary Pediatrics, vol. 13, no. 2, Jan. 2026, pp. 342-5, doi:10.18203/2349-3291.ijcp20260114.