Clinical features and genetic variations of severe neonatal hyperbilirubinemia: Five case reports

por Lin, Fen, Xu, Jian-Xin, Wu, Yong-Hao, Ma, Yu-Bin, Yang, Li-Ye
Publicado 2022

Etiology analysis for term newborns with severe hyperbilirubinemia in eastern Guangdong of China

por Xu, Jia-Xin, Lin, Fen, Wu, Yong-Hao, Chen, Zi-Kai, Ma, Yu-Bin, Yang, Li-Ye
Publicado 2023

UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China

por Yang, Hui, Lin, Fen, Chen, Zi-kai, Zhang, Lin, Xu, Jia-Xin, Wu, Yong-Hao, Gu, Jing-Ying, Ma, Yu-Bin, Li, Jian-Dong, Yang, Li-Ye
Publicado 2021

UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice

por Yang, Zhe, Lin, Fen, Xu, Jia-Xin, Yang, Hui, Wu, Yong-Hao, Chen, Zi-Kai, Xie, He, Huang, Bin, Lin, Wei-Hao, Wu, Jian-Peng, Ma, Yu-Bin, Li, Jian-Dong, Yang, Li-Ye
Publicado 2022