APA (7th ed.) Citation

Linda R. Wang MD, Aleksandar Radonjic BSc, Allison A. Dilliott BSc, Adam D. McIntyre BSc, & Robert A. Hegele MD, F. (2018). A De Novo Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome. SAGE Publishing.

Chicago Style (17th ed.) Citation

Linda R. Wang MD, Aleksandar Radonjic BSc, Allison A. Dilliott BSc, Adam D. McIntyre BSc, and FRCPC Robert A. Hegele MD. A De Novo Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome. SAGE Publishing, 2018.

MLA (9th ed.) Citation

Linda R. Wang MD, et al. A De Novo Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome. SAGE Publishing, 2018.