APA (7th ed.) Citation

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.) Citation

SL, 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.) Citation

SL, 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.

Warning: These citations may not always be 100% accurate.