1. The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43. (19th April 2013) Authors: Hodgkinson, KA; Connors, SP; Merner, N; Haywood, A; Young, T‐L; McKenna, WJ; Gallagher, B; Curtis, F; Bassett, AS; Parfrey, PS Journal: Clinical genetics Issue: Volume 83:Number 4(2013:Apr.) Page Start: 321 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation. (19th April 2013) Authors: Stuckless, S; Green, J; Dawson, L; Barrett, B; Woods, MO; Dicks, E; Parfrey, PS Journal: Clinical genetics Issue: Volume 83:Number 4(2013:Apr.) Page Start: 359 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation. (7th August 2012) Authors: Stuckless, S; Green, J; Dawson, L; Barrett, B; Woods, MO; Dicks, E; Parfrey, PS Journal: Clinical genetics Issue: Volume 83:Number 4(2013:Apr.) Page Start: 359 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43. (13th August 2012) Authors: Hodgkinson, KA; Connors, SP; Merner, N; Haywood, A; Young, T‐L; McKenna, WJ; Gallagher, B; Curtis, F; Bassett, AS; Parfrey, PS Journal: Clinical genetics Issue: Volume 83:Number 4(2013:Apr.) Page Start: 321 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗