1. A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. Issue 12 (16th April 2021) Authors: Martinelli, Angela; Rice, Mabel L; Talcott, Joel B; Diaz, Rebeca; Smith, Shelley; Raza, Muhammad Hashim; Snowling, Margaret J; Hulme, Charles; Stein, John; Hayiou-Thomas, Marianna E; Hawi, Ziarih; Kent, Lindsey; Pitt, Samantha J; Newbury, Dianne F; Paracchini, Silvia Journal: Human molecular genetics Issue: Volume 30:Issue 12(2021) Page Start: 1160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Evaluation of the implementation of a best practice gestational diabetes model of care in two Australian metropolitan services. Issue 1 (8th March 2022) Authors: Wilkinson, Shelley A.; Palmer, Michelle; Smith, Shelley; Porteous, Helen; McCray, Sally Journal: JBI evidence implementation Issue: Volume 20:Issue 1(2022) Page Start: 10 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Investigating the effects of copy number variants on reading and language performance. Issue 1 (December 2016) Authors: Gialluisi, Alessandro; Visconti, Alessia; Willcutt, Erik; Smith, Shelley; Pennington, Bruce; Falchi, Mario; DeFries, John; Olson, Richard; Francks, Clyde; Fisher, Simon Journal: Journal of neurodevelopmental disorders Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗