Truty, R., Patil, N., Sankar, R., Sullivan, J., Millichap, J., Carvill, G., . . . Aradhya, S. (2019). Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy. Epilepsia Open.
Chicago-стиль цитированияTruty, Rebecca, et al. "Possible Precision Medicine Implications From Genetic Testing Using Combined Detection of Sequence and Intragenic Copy Number Variants in a Large Cohort With Childhood Epilepsy." Epilepsia Open 2019.
MLA-цитированиеTruty, Rebecca, et al. "Possible Precision Medicine Implications From Genetic Testing Using Combined Detection of Sequence and Intragenic Copy Number Variants in a Large Cohort With Childhood Epilepsy." Epilepsia Open 2019.