Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates
- 1 August 2000
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 356 (9230) , 652-653
- https://doi.org/10.1016/s0140-6736(00)02610-6
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Gilbert syndrome accelerates development of neonatal jaundiceThe Journal of Pediatrics, 1998
- Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemiaProceedings of the National Academy of Sciences, 1997
- Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndromeThe Lancet, 1996
- The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's SyndromeNew England Journal of Medicine, 1995