SL, S., S, H., A, M., T, M. M., R, P., SC, R., . . . SE, H. (2017). Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy. Cytogenetic and genome research, 152(2), 105. https://doi.org/10.1159/000478921
Chicago Style (17th ed.) CitationSL, Santoro, Hashimoto S, McKinney A, Mihalic Mosher T, Pyatt R, Reshmi SC, Astbury C, and Hickey SE. "Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome Due to Uniparental Disomy." Cytogenetic and Genome Research 152, no. 2 (2017): 105. https://doi.org/10.1159/000478921.
MLA (9th ed.) CitationSL, Santoro, et al. "Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome Due to Uniparental Disomy." Cytogenetic and Genome Research, vol. 152, no. 2, 2017, p. 105, https://doi.org/10.1159/000478921.