Author:
Skierka Jennifer M.,Kotzer Katrina E.,Lagerstedt Susan A.,O'Kane Dennis J.,Baudhuin Linnea M.
Subject
Pediatrics, Perinatology and Child Health
Reference42 articles.
1. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias;Clarke;Clin Chim Acta,1997
2. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler–Najjar and Gilbert syndromes: correlation of genotype to phenotype;Kadakol;Hum Mutat,2000
3. Management of hyperbilirubinemia and prevention of kernicterus in 20 patients with Crigler–Najjar disease;Strauss;Eur J Pediatr,2006
4. Online Mendelian Inheritance in Man, OMIM. Johns Hopkins University, Baltimore, MD. MIM Number: {191740}. Available at: http://omim.org. Accessed December 14, 2012.
5. Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency: evidence for genetic heterogeneity;Arias;Trans Assoc Am Physicians,1968
Cited by
40 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献