Kaplan, M <br/><br/>
Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.  [electronic resource] 

 -  Journal of perinatology : official journal of the California Perinatal Association  Dec 2001 
 - S30-4; discussion S35-9 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0743-8346 
<br/><br/><label>Standard No.: </label>10.1038/sj.jp.7210630  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Bilirubin--metabolism<br/>Gilbert Disease--complications<br/>Glucuronosyltransferase--metabolism<br/>Glycogen Storage Disease Type I--complications<br/>Hemolysis<br/>Humans<br/>Infant, Newborn<br/>Jaundice, Neonatal--etiology<br/>Liver--metabolism<br/>Promoter Regions, Genetic