Lowther, C., Speevak, M., Armour, C. M., Goh, E. S., Graham, G. E., Li, C., . . . Bassett, A. S. (2016). Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. Genet Med.

Lowther, Chelsea, et al. "Molecular Characterization of NRXN1 Deletions From 19,263 Clinical Microarray Cases Identifies Exons Important for Neurodevelopmental Disease Expression." Genet Med 2016.

Lowther, Chelsea, et al. "Molecular Characterization of NRXN1 Deletions From 19,263 Clinical Microarray Cases Identifies Exons Important for Neurodevelopmental Disease Expression." Genet Med 2016.