Original articleClinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia
Under a Creative Commons license
open access
Key Words
G6PD deficiency
genetic diagnosis
neonatal hyperbilirubinemia
thalassemia
UGT1A1 variant
Cited by (0)
Copyright © 2015, Taiwan Pediatric Association. Published by Elsevier Taiwan LLC.