Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome [2]

European Journal of Pediatrics

Volumn 160, Issue 3, 2001, Pages 195-

  Kaplan, Michael ^a   Hammerman, Cathy ^a   Beutler, Ernest ^b  

^a SHAARE ZEDEK MEDICAL CENTER   (Israel)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUCURONOSYLTRANSFERASE;

CLINICAL ARTICLE; DISEASE ASSOCIATION; GENOTYPE; GILBERT DISEASE; GLYCOGEN STORAGE DISEASE TYPE 1; HOMOZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERBILIRUBINEMIA; INFANT; LETTER; POPULATION GENETICS; PRIORITY JOURNAL; RACE DIFFERENCE; RISK ASSESSMENT; STATISTICAL ANALYSIS;

EID: 0035104864     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/PL00008422     Document Type: Letter

References (2)

1. Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome
2. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia