1. An interesting case of ptosis in an infant. Issue 6 (20th February 2015) Authors: Groves, Helen Elizabeth; Christie, Sharon; McGinnity, Gerry; Hanrahan, Donncha; Thompson, Andrew Journal: Archives of disease in childhood Issue: Volume 100:Issue 6(2015) Page Start: 294 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Answers to Epilogue. Issue 6 (19th November 2015) Authors: Groves, Helen Elizabeth; Christie, Sharon; McGinnity, Gerry; Hanrahan, Donncha; Thompson, Andrew Journal: Archives of disease in childhood Issue: Volume 100:Issue 6(2015) Page Start: 336 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. (16th January 2015) Authors: Crow, Yanick J.; Chase, Diana S.; Lowenstein Schmidt, Johanna; Szynkiewicz, Marcin; Forte, Gabriella M.A.; Gornall, Hannah L.; Oojageer, Anthony; Anderson, Beverley; Pizzino, Amy; Helman, Guy; Abdel‐Hamid, Mohamed S.; Abdel‐Salam, Ghada M.; Ackroyd, Sam; Aeby, Alec; Agosta, Guillermo; Albin, Cath... Journal: American journal of medical genetics Issue: Volume 167:Number 2(2015:Feb.) Page Start: 296 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Towards the identification of a genetic basis for Landau‐Kleffner syndrome. Issue 6 (14th May 2014) Authors: Conroy, Judith; McGettigan, Paul A.; McCreary, Dara; Shah, Naisha; Collins, Kevin; Parry‐Fielder, Bronwyn; Moran, Margaret; Hanrahan, Donncha; Deonna, Thierry W.; Korff, Christian M.; Webb, David; Ennis, Sean; Lynch, Sally A.; King, Mary D. Journal: Epilepsia Issue: Volume 55:Issue 6(2014:Jun.) Page Start: 858 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗