Brown, R., Lee, H., Eskin, A., Kichaev, G., Lohmueller, K. E., Reversade, B., . . . Pasaniuc, B. (2016). Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders. Eur J Hum Genet.
Citación estilo ChicagoBrown, Robert, Hane Lee, Ascia Eskin, Gleb Kichaev, Kirk E. Lohmueller, Bruno Reversade, Stanley F. Nelson, and Bogdan Pasaniuc. "Leveraging Ancestry to Improve Causal Variant Identification in Exome Sequencing for Monogenic Disorders." Eur J Hum Genet 2016.
Cita MLABrown, Robert, et al. "Leveraging Ancestry to Improve Causal Variant Identification in Exome Sequencing for Monogenic Disorders." Eur J Hum Genet 2016.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.