Normand, E. A., Braxton, A., Nassef, S., Ward, P. A., Vetrini, F., He, W., . . . Yang, Y. (2018). Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder. Genome Medicine, 10(1), 1. https://doi.org/10.1186/s13073-018-0582-x
Chicago Style (17th ed.) CitationNormand, Elizabeth A., et al. "Clinical Exome Sequencing for Fetuses with Ultrasound Abnormalities and a Suspected Mendelian Disorder." Genome Medicine 10, no. 1 (2018): 1. https://doi.org/10.1186/s13073-018-0582-x.
MLA (9th ed.) CitationNormand, Elizabeth A., et al. "Clinical Exome Sequencing for Fetuses with Ultrasound Abnormalities and a Suspected Mendelian Disorder." Genome Medicine, vol. 10, no. 1, 2018, p. 1, https://doi.org/10.1186/s13073-018-0582-x.