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- [1] Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2011, 24 (02): : 313 - 316
- [2] G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2012, 25 (09): : 1833 - 1834
- [4] Frequency of G71R and Detection of a Novel Mutation in Exon 1 of the UGT1A1 Gene in a Malay Population INTERNATIONAL MEDICAL JOURNAL, 2012, 19 (02): : 93 - 97
- [7] Frequencies of A(TA)7TAA, G71R, and G493R mutations of the UGT1A1 gene in the Malaysian population BIOLOGY OF THE NEONATE, 2006, 89 (03): : 171 - 176
- [9] UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice FRONTIERS IN PEDIATRICS, 2022, 10
- [10] Prolonged neonatal hyperbilirubinemia associated with a UGT1A1 gene mutation ANALES DE PEDIATRIA, 2010, 72 (06): : 449 - 450