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» Single nucleotide polymorphisms (SNPs) and mutations in human genes
Thrombophilia and hyperhomocysteinemia
Metabolic disorder
Cardiovascular diseases
Predicting the success of HCV therapy
Gilbert's syndrome
Reproductive function
Hereditary breast and ovarian cancer
Hereditary HFE-associated hemochromatosis (hemochromatosis type I)
Autoimmune disease
Pharmacogenetics of warfarin