1. Counselling issues in familial hypertrophic cardiomyopathy. Issue 3 (March 1998) Authors: Yu, B; French, J A; Jeremy, R W; French, P; McTaggart, D R; Nicholson, M R; Semsarian, C; Richmond, D R; Trent, R J Journal: Journal of medical genetics Issue: Volume 35:Issue 3(1998) Page Start: 183 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene. Issue 3 (March 1998) Authors: Yu, B; French, J A; Carrier, L; Jeremy, R W; McTaggart, D R; Nicholson, M R; Hambly, B; Semsarian, C; Richmond, D R; Schwartz, K; Trent, R J Journal: Journal of medical genetics Issue: Volume 35:Issue 3(1998) Page Start: 205 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene. Issue 2 (August 1994) Authors: al-Mahdawi, S; Chamberlain, S; Chojnowska, L; Michalak, E; Nihoyannopoulos, P; Ryan, M; Kusnierczyk, B; French, J A; Gilligan, D M; Cleland, J Journal: Heart Issue: Volume 72:Issue 2(1994) Page Start: 105 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗