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22. [Gilbert's syndrome: hyperbilirubinemia enemy or friend]. Xiang GQ; Sun FR; Wang BY Zhonghua Gan Zang Bing Za Zhi; 2021 Oct; 29(10):1024-1027. PubMed ID: 34814402 [TBL] [Abstract][Full Text] [Related]
23. Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter. Hsieh TY; Shiu TY; Huang SM; Lin HH; Lee TC; Chen PJ; Chu HC; Chang WK; Jeng KS; Lai MM; Chao YC Pharmacogenet Genomics; 2007 Apr; 17(4):229-36. PubMed ID: 17496722 [TBL] [Abstract][Full Text] [Related]
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25. UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias. Khan S; Irfan M; Sher G; Zubaida B; Alvi MA; Yasinzai M; Naeem M Ann Hum Genet; 2013 Nov; 77(6):482-7. PubMed ID: 23992562 [TBL] [Abstract][Full Text] [Related]
26. [UGT1A1 gene mutation spectrum with indirect hyperbilirubinemia in children]. Shen Y; Guo HM; Zheng YC; Zheng BX; Yan KL; Kong GP; Lin Q; Jin Y; Liu ZF; Li M Zhonghua Gan Zang Bing Za Zhi; 2024 Feb; 32(2):119-124. PubMed ID: 38514260 [No Abstract] [Full Text] [Related]
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28. Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Kumar D; Parakh A; Sharma S J Pediatr Hematol Oncol; 2012 Jan; 34(1):54-6. PubMed ID: 22134611 [TBL] [Abstract][Full Text] [Related]
29. Gilbert syndrome accelerates development of neonatal jaundice. Bancroft JD; Kreamer B; Gourley GR J Pediatr; 1998 Apr; 132(4):656-60. PubMed ID: 9580766 [TBL] [Abstract][Full Text] [Related]
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34. Frequency of the UGT1A1*28 Polymorphism in a Romanian Cohort of Gilbert Syndrome Individuals. Radoi VE; Ursu RI; Poenaru E; Arsene C; Bohiltea CL; Bohiltea R J Gastrointestin Liver Dis; 2017 Mar; 26(1):25-28. PubMed ID: 28338110 [TBL] [Abstract][Full Text] [Related]