Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Birth Weight and G6PD[original query] |
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Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia. Gastroenterology 2002 Jul 123 (1): 127-33. Huang Ching-Shan, Chang Pi-Feng, Huang May-Jen, Chen En-Sung, Chen Wu-Char |
Comparison of detection of glucose-6-phosphate dehydrogenase deficiency using fluorescent spot test, enzyme assay and molecular method for prediction of severe neonatal hyperbilirubinaemia. Singapore medical journal 2009 Jan 50 (1): 62-7. Wang F L, Boo N Y, Ainoon O, Wong M |
Identifying term breast-fed infants at risk of significant hyperbilirubinemia. Pediatric research 2013 Oct 74 (4): 408-12. Chang Pi-Feng, Lin Yu-Cheng, Liu Kevin, Yeh Shu-Jen, Ni Yen-Hsu |
Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates. Journal of tropical pediatrics 2013 Aug 59 (4): 280-5. Wong Feiliang, Boo NemYun, Othman Aino |
UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice. Frontiers in pediatrics 2023 1 10 1080212. Yang Zhe, Lin Fen, Xu Jia-Xin, Yang Hui, Wu Yong-Hao, Chen Zi-Kai, Xie He, Huang Bin, Lin Wei-Hao, Wu Jian-Peng, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
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