Wood, A. R., Perry, J. R. B., Tanaka, T., Hernandez, D. G., Zheng, H., Melzer, D., . . . Frayling, T. M. (2013). Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation. Public Library of Science.
Stile di citazione ChicagoWood, Andrew R., et al. Imputation of Variants From the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected By HapMap Based Imputation. Public Library of Science, 2013.
Citazione MLAWood, Andrew R., et al. Imputation of Variants From the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected By HapMap Based Imputation. Public Library of Science, 2013.