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Search Results for: Hereditary Genetics
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NOX Subunit Gene Polymorphisms and the Risk of Chronic Artery Disease in Type 2 Diabetes Patients
Polymorphic variants of glutathione reductase–new genetic markers of predisposition to type 2 diabetes mellitus
Association of ATG5 gene polymorphism with Parkinson’s disease in a Han Chinese population
IL1R2 polymorphisms and their interaction are associated with osteoporosis susceptibility in the Chinese Han population
Risk of migraine contributed by genetic polymorphisms of ANKDD1B gene: a case–control study based on Chinese Han population
Association and Gene–Gene Interactions Study of Late-Onset Alzheimer’s Disease in the Russian Population
Placental cadmium, placental genetic variations, and birth size
Lrp6 Genotype affects Individual Susceptibility to Nonalcoholic Fatty Liver Disease and Silibinin Therapeutic Response via Wnt/β-catenin-Cyp2e1 Signaling
Vitamin D-related polymorphisms and vitamin D levels as risk biomarkers of COVID-19 disease severity
PDX1 and MC4R genetic polymorphisms are associated with type 2 diabetes mellitus risk in the Chinese Han population
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