Yu-Bin Ma

Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

F. Lin, Zhao-yun Luo, Li-ye Yang, 2021, BMC Pediatrics.

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

F. Lin, Lin Zhang, Hui Yang, 2021, BMC Pediatrics.

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

F. Lin, Yong-Hao Wu, Zi-kai Chen, 2023, World journal of clinical cases.

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

F. Lin, Li-ye Yang, Yong-Hao Wu, 2022, World Journal of Clinical Cases.

Red Blood Cell Membrane-Related Gene Variants and Clinical Risk Factors in Chinese Neonates with Hyperbilirubinemia

F. Lin, Yong-Hao Wu, Zi-kai Chen, 2023, Neonatology.

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

F. Lin, Wei-Hao Lin, He Xie, 2022, Frontiers in Pediatrics.

Covid-19 omicron variant infection in neonates of Guangdong province-a report of 52 cases

F. Lin, Guang Zeng, Li-ye Yang, 2023, Frontiers in Pediatrics.