Guo, X H <br/><br/>
Analysis of uridine diphosphate glucuronosyl transferase 1A1 gene mutations in neonates with unconjugated hyperbilirubinemia.  [electronic resource] 

 -  Genetics and molecular research : GMR  May 2016 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1676-5680 
<br/><br/><label>Standard No.: </label>10.4238/gmr.15028373  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Bilirubin--blood<br/>Female<br/>Gene Frequency<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Glucuronosyltransferase--genetics<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Hyperbilirubinemia, Hereditary--blood<br/>Infant, Newborn<br/>Male<br/>Mutation<br/>Polymorphism, Single Nucleotide