Lopez Martinolich, M., Northrup, H., Mancias, P., Hillman, P., Rao, K., & Mowrey, K. (2022). Identification of a novel microdeletion causative of Nance‐Horan syndrome. Molecular Genetics & Genomic Medicine, 10(3), 1. https://doi.org/10.1002/mgg3.1879
Chicago Style (17th ed.) CitationLopez Martinolich, Mariana, Hope Northrup, Pedro Mancias, Paul Hillman, Kavya Rao, and Kate Mowrey. "Identification of a Novel Microdeletion Causative of Nance‐Horan Syndrome." Molecular Genetics & Genomic Medicine 10, no. 3 (2022): 1. https://doi.org/10.1002/mgg3.1879.
MLA (9th ed.) CitationLopez Martinolich, Mariana, et al. "Identification of a Novel Microdeletion Causative of Nance‐Horan Syndrome." Molecular Genetics & Genomic Medicine, vol. 10, no. 3, 2022, p. 1, https://doi.org/10.1002/mgg3.1879.