Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Hemolysis and ABO[original query] |
---|
Clinical features and genetic variations of severe neonatal hyperbilirubinemia: Five case reports. World journal of clinical cases 2022 Jul 10 (20): 6999-7005. Lin Fen, Xu Jian-Xin, Wu Yong-Hao, Ma Yu-Bin, Yang Li- |
Association of haptoglobin levels with age, parasite density, and haptoglobin genotype in a malaria-endemic area of Gabon. The American journal of tropical medicine and hygiene 2006 Jan 74 (1): 26-30. Fowkes Freya J I, Imrie Heather, Migot-Nabias Florence, Michon Pascal, Justice Anita, Deloron Phillipe, Luty Adrian J F, Day Karen |
Passenger lymphocyte syndrome in ABO and Rhesus D minor mismatched liver and kidney transplantation: A prospective analysis. Human immunology 2015 Jun 76 (6): 447-52. ElAnsary Mervat, Hanna Mariam Onsy F, Saadi Gamal, ElShazly Mostafa, Fadel Fatina I, Ahmed Hanan AbdElAziz, Aziz Amr Mostafa, ElSharnouby Amal, Kandeel Mona MohiElDin |
Study of Gilbert's Syndrome-Associated UGT1A1 Polymorphism in Jaundiced Neonates of ABO Incompatibility Hemolysis Disease. American journal of perinatology 2019 May . Yu Yingfang, Du Lizhong, Chen An, Chen Lih |
UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China. BMC pediatrics 2021 06 21 (1): 259. Yang Hui, Lin Fen, Chen Zi-Kai, Zhang Lin, Xu Jia-Xin, Wu Yong-Hao, Gu Jing-Ying, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
- Content source: