1. A diagnostic dilemma: variant Bernard–Soulier syndrome, a difficult clinical and genetic diagnosis. (31st July 2015) Authors: Okoli, S.; Madan, B.; Mwirigi, A.; Moore, G.; Drew, A.; Mitchell, M. J.; Cutler, J. A. Journal: Haemophilia Issue: Volume 21:Number 6(2015:Nov.) Page Start: e510 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. The first report of a multi‐exon duplication in the F9 gene causative of severe haemophilia B. (17th July 2015) Authors: Wheeler, R. B.; Cutler, J. A.; Alamelu, J.; Mitchell, M. J. Journal: Haemophilia Issue: Volume 21:Number 5(2015:Sep.) Page Start: e433 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗