Associated Papers
Precise diagnosis of a hereditary spherocytosis patient with complicated hematological phenotype.
Liang G et al.
Molecular Genetics and Genomics : Mgg, 2024
UGT1A1 sequence variants associated with risk of adult hyperbilirubinemia: a quantitative analysis.
Chen Z et al.
Gene, 2014
Differences in frequencies of UGT1A9, 1A7, and 1A1 genetic polymorphisms in Chinese Tibetan versus Han Chinese populations.
Yan W et al.
Genetics and Molecular Research : Gmr, 2013
Comprehensive analysis of UGT1A1 genetic polymorphisms in Chinese Tibetan and Han populations.
Zhang X et al.
Biochemical Genetics, 2012
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