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Query Trace: Genetic Diseases, Inborn and CYBA[orginal query]

Prediction of features of the course of chronic hepatitis C using Bayesian networks. Terapevticheskii arkhiv 2019 Mar 91 (2): 32-39. Samokhodskaya L M, Starostina E E, Sulimov A V, Krasnova ? N, Rosina T P, Avdeev V G, Savkin I A, Sulimov V B, Mukhin N A, Tkachuk V A, Sadovnichii V Similar articles in PubMed
Polymorphism in the HMOX1 gene is associated with high levels of fetal hemoglobin in Brazilian patients with sickle cell anemia. Hemoglobin 2013 37 (4): 315-24. Gil Gislene P, Ananina Galina, Oliveira Mariana B, Costa Fernando F, Silva Márcio J, Santos Magnun N N, Bezerra Marcos A C, Hatzlhofer Betânia L D, Araujo Aderson S, Melo Mônica Similar articles in PubMed
NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2. Gut 2012 Jul 61 (7): 1028-35. Muise Aleixo M, Xu Wei, Guo Cong-Hui, Walters Thomas D, Wolters Victorien M, Fattouh Ramzi, Lam Grace Y, Hu Pingzhao, Murchie Ryan, Sherlock Mary, Gana Juan Cristóbal, , Russell Richard K, Glogauer Michael, Duerr Richard H, Cho Judy H, Lees Charlie W, Satsangi Jack, Wilson David C, Paterson Andrew D, Griffiths Anne M, Silverberg Mark S, Brumell John Similar articles in PubMed
Genetic variants of TP53 and EPHX1 in Leber's hereditary optic neuropathy and their relationship to age at onset. Japanese journal of ophthalmology 0 49 (2): 121-6. Ishikawa Karin, Funayama Tomoyo, Ohde Hisao, Inagaki Yoko, Mashima Yukihi Similar articles in PubMed