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The Journal of Maternal-Fetal & Neonatal Medicine Volume 30, 2017 - Issue 22
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Original Article

The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice

Hülya Halisa Department of Pediatrics, Faculty of Medicine, Pamukkale University, Denizli, Turkey; View further author information
,
Hacer Erginb Department of Pediatrics, Division of Neonatology, Faculty of Medicine, Pamukkale University, Denizli, Turkey; Correspondence[email protected]
View further author information
,
Aylin Köselerc Department of Biophysics, Faculty of Medicine, Pamukkale University, Denizli, TurkeyView further author information
&
Erol Ömer Atalayc Department of Biophysics, Faculty of Medicine, Pamukkale University, Denizli, TurkeyView further author information
Pages 2658-2664 | Received 05 May 2016, Accepted 11 Nov 2016, Published online: 06 Feb 2017

Citations (6)

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Read on this site (2)

Yuqi Yang, Yu Wang, Lingna Zhou, Wei Long, Bin Yu & Huaiyan Wang. (2022) Molecular Genetic Screening of Neonatal Intensive Care Units: Hyperbilirubinemia as an Example. The Application of Clinical Genetics 15, pages 39-48.
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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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Articles from other publishers (4)

Jon F. Watchko. (2022) ABO hemolytic disease of the newborn: a need for clarity and consistency in diagnosis. Journal of Perinatology 43:2, pages 242-247.
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Hui Yang, Fen Lin, Zi-kai Chen, Lin Zhang, Jia-Xin Xu, Yong-Hao Wu, Jing-Ying Gu, Yu-Bin Ma, Jian-Dong Li & Li-Ye Yang. (2021) UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China. BMC Pediatrics 21:1.
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Zijin Li, Li Song & Lihong Hao. (2020) The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility. BMC Medical Genetics 21:1.
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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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