Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study.

MLA

Dyment, D. A., et al. “Whole-Exome Sequencing Broadens the Phenotypic Spectrum of Rare Pediatric Epilepsy: A Retrospective Study.” Clinical Genetics, vol. 88, no. 1, July 2015, pp. 34–40. EBSCOhost, https://doi.org/10.1111/cge.12464.

APA

Dyment, D. A., Tétreault, M., Beaulieu, C. L., Hartley, T., Ferreira, P., Chardon, J. W., Marcadier, J., Sawyer, S. L., Mosca, S. J., Innes, A. M., Parboosingh, J. S., Bulman, D. E., Schwartzentruber, J., Majewski, J., Tarnopolsky, M., & Boycott, K. M. (2015). Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study. Clinical Genetics, 88(1), 34–40. https://doi.org/10.1111/cge.12464

Chicago

Dyment, D A, M Tétreault, C L Beaulieu, T Hartley, P Ferreira, J W Chardon, J Marcadier, et al. 2015. “Whole-Exome Sequencing Broadens the Phenotypic Spectrum of Rare Pediatric Epilepsy: A Retrospective Study.” Clinical Genetics 88 (1): 34–40. doi:10.1111/cge.12464.