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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 4, 2023. (Total: 217641Documents)
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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-
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