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Original Article

Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients

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Pages 313-316 | Received 02 Feb 2010, Accepted 27 Apr 2010, Published online: 08 Jun 2010

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Hassan Mehrad-Majd, Monir Sadat Haerian, Javad Akhtari, Yalda Ravanshad, Anoush Azarfar & Gholamali Mamouri. (2019) Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis. The Journal of Maternal-Fetal & Neonatal Medicine 32:10, pages 1575-1585.
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Hülya Halis, Hacer Ergin, Aylin Köseler & Erol Ömer Atalay. (2017) The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice. The Journal of Maternal-Fetal & Neonatal Medicine 30:22, pages 2658-2664.
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Articles from other publishers (4)

Jing Wang, Jiansong Yin, Mei Xue, Jun Lyu & Yu Wan. (2020) Roles of UGT1A1 Gly71Arg and TATA promoter polymorphisms in neonatal hyperbilirubinemia: A meta-analysis. Gene 736, pages 144409.
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Xiao-Jing Wu, Dan-Ni Zhong, Xiang-Zhi Xie, De-Zhi Ye & Zong-Yan Gao. (2015) UGT1A1 gene mutations and neonatal hyperbilirubinemia in Guangxi Heiyi Zhuang and Han populations. Pediatric Research 78:5, pages 585-588.
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Zibi YuKaichang ZhuLi WangYing LiuJianmei Sun. (2015) Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis. Medical Science Monitor 21, pages 3104-3114.
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Jun Long, Shaofang Zhang, Xiaoyan Fang, Yuyuan Luo & Jiebo Liu. (2011) Association of neonatal hyperbilirubinemia with uridine diphosphate-glucuronosyltransferase 1A1 gene polymorphisms: Meta-analysis. Pediatrics International 53:4, pages 530-540.
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