Park, J., Levin, M. G., Haggerty, C. M., Hartzel, D. N., Judy, R., Kember, R. L., . . . Rader, D. J. (2019). A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes. Genet Med.
Citação norma ChicagoPark, Joseph, et al. "A Genome-first Approach to Aggregating Rare Genetic Variants in LMNA for Association With Electronic Health Record Phenotypes." Genet Med 2019.
Deismireacht MLAPark, Joseph, et al. "A Genome-first Approach to Aggregating Rare Genetic Variants in LMNA for Association With Electronic Health Record Phenotypes." Genet Med 2019.
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