Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates

Haematologica

Volumn 84, Issue 2, 1999, Pages 99-102

  Iolascon, Achille ^a   Faienza, Maria Felicia ^b   Perrotta, Silverio ^b   Meloni, Gian Franco ^b   Ruggiu, Giuseppina ^b   Miraglia Del Giudice, Emanuele ^b  

^a POLICLINICO   (Italy)

^b NONE

Author keywords

Gilbert syndrome; Glucose 6 phosphate dehydrogenase deficiency; Hyperbilirubinemia; Neonates; Uridine diphosphate glucuronosyltransferase

Indexed keywords

BILIRUBIN; DNA; GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

ARTICLE; CONTROLLED STUDY; GENE; GENOTYPE; GILBERT DISEASE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HUMAN; HYPERBILIRUBINEMIA; JAUNDICE; MAJOR CLINICAL STUDY; MALE; NEWBORN; POLYMERASE CHAIN REACTION; TATA BOX;

EID: 0032859356     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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