Glucose-6-phosphate dehydrogenase deficiency among newborns with indirect hyperbilirubinaemia

Screening for G6PD deficiency in neonates

Genotype and phenotype correlation in glucose-6- phosphate dehydrogenase deficiency

Assessment of the efficacy of haptoglobin as a detector for neonatal jaundice

Hyperbilirubinemia in a neonatal intensive care unit : Incidence and etiology

Complications and outcome of exchange transfusion in neonatal hyperbilirubinemia

Detection of inborn errors of metabolism among pediatric patients admitted to pediatric ICU

DNA sequencing of uncharacterized β–globin gene mutations in β–thalassaemia in children

Transcutaneous bilirubinometery : Its role in the assessment of neonatal jaundice with comparable precision with serum bilirubin

DNA sequencing of uncharacterized beta–globin gene mutations in beta–thalassaemia in children