Rare presentation of subclavian artery isolation in a neonate with a family history of aortic arch anomalies. by Ashrafian, H, Tsang, V, Kostolny, M

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency. by Marston, S, Copeland, O, Jacques, A, Livesey, K, Tsang, V, McKenna, W, Jalilzadeh, S, Carballo, S, Redwood, C, Watkins, H

Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathy. by Hoskins, A, Jacques, A, Bardswell, S, McKenna, W, Tsang, V, dos Remedios, C, Ehler, E, Adams, K, Jalilzadeh, S, Avkiran, M, Watkins, H, Redwood, C, Marston, S, Kentish, J