APA (7th ed.) Citation

Lowther, C., Speevak, M., Armour, C. M., Goh, E. S., Graham, G. E., Li, C., . . . Bassett, A. S. (2017). Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. Genetics in medicine, 19(1), 53-61. https://doi.org/10.1038/gim.2016.54

Chicago Style (17th ed.) Citation

Lowther, Chelsea, et al. "Molecular Characterization of NRXN1 Deletions from 19,263 Clinical Microarray Cases Identifies Exons Important for Neurodevelopmental Disease Expression." Genetics in Medicine 19, no. 1 (2017): 53-61. https://doi.org/10.1038/gim.2016.54.

MLA (9th ed.) Citation

Lowther, Chelsea, et al. "Molecular Characterization of NRXN1 Deletions from 19,263 Clinical Microarray Cases Identifies Exons Important for Neurodevelopmental Disease Expression." Genetics in Medicine, vol. 19, no. 1, 2017, pp. 53-61, https://doi.org/10.1038/gim.2016.54.