Whiffin, N., Roberts, A. M., Minikel, E., Zappala, Z., Walsh, R., O’Donnell-Luria, A. H., . . . Ware, J. S. (2019). Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of Genetic Architecture. Am J Hum Genet.
Čikaški stil citiranjaWhiffin, Nicola, et al. "Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of Genetic Architecture." Am J Hum Genet 2019.
MLA način citiranjaWhiffin, Nicola, et al. "Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of Genetic Architecture." Am J Hum Genet 2019.
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