Associated Papers
Etiology analysis and G6PD deficiency for term infants with jaundice in Yangjiang of western Guangdong.
Yang YK et al.
Frontiers in Pediatrics, 2023
Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong.
Xu JX et al.
Bmc Pediatrics, 2021
Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.
Boo NY et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2009
[Identification of G6PD gene variants from Hakka population in Guangdong province].
Yu GL et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2004
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