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Search Results for: Hereditary Genetics
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Associated with Benign Prostatic Hyperplasia Risk in a Chinese Population
Association between paraoxonase gene and stroke in the Han Chinese population
Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a Northern European family population
Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population
JAK1, but not JAK2 and STAT3, confers susceptibility to Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population
Common genetic variants regulating ADD3 gene expression alter biliary atresia risk:
CNTNAP2 polymorphisms and structural brain connectivity: A diffusion-tensor imaging study:
Single-nucleotide Polymorphism and Haplotypes of TNIP1 Associated with Systemic Lupus Erythematosus in a Chinese Han Population
Polymorphisms in DNA repair genes and susceptibility to glioma in a Chinese population
Inclusion of Genotype with Fundus Phenotype Improves Accuracy of Predicting Choroidal Neovascularization and Geographic Atrophy
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