1. Intracranial haemorrhage in children with inherited bleeding disorders in the UK 2003‐2015: A national cohort study. Issue 4 (10th April 2018) Authors: Chalmers, E. A.; Alamelu, J.; Collins, P. W.; Mathias, M.; Payne, J.; Richards, M.; Tunstall, O.; Williams, M.; Palmer, B.; Mumford, A. Journal: Haemophilia Issue: Volume 24:Issue 4(2018) Page Start: 641 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders. (27th January 2015) Authors: Leo, V. C.; Morgan, N. V.; Bem, D.; Jones, M. L.; Lowe, G. C.; Lordkipanidzé, M.; Drake, S.; Simpson, M. A.; Gissen, P.; Mumford, A.; Watson, S. P.; Daly, M. E.; the UK GAPP Study Group Journal: Journal of thrombosis and haemostasis Issue: Volume 13:Number 4(2015:Apr.) Page Start: 643 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗