1. High frequency of APOB gene mutations causing familial hypobetalipoproteinaemia in patients of Dutch and Spanish descent. Issue 4 (1st April 2005) Authors: Fouchier, S W; Sankatsing, R R; Peter, J; Castillo, S; Pocovi, M; Alonso, R; Kastelein, J J P; Defesche, J C Journal: Journal of medical genetics Issue: Volume 42:Issue 4(2005) Page Start: e23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Parental attitude towards genetic testing for familial hypercholesterolaemia in children. Issue 9 (1st September 2002) Authors: Umans-Eckenhausen, M A W; Oort, F J; Ferenschild, K C M P; Defesche, J C; Kastelein, J J P; de Haes, J C J M Journal: Journal of medical genetics Issue: Volume 39:Issue 9(2002) Page Start: e49 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Results from a family and DNA based active identification programme for familial hypercholesterolaemia. Issue 7 (1st July 2001) Authors: ten Asbroek, A H A; de Mheen, P J Marang-van; Defesche, J C; Kastelein, J J P; Gunning-Schepers, L J Journal: Journal of epidemiology and community health Issue: Volume 55:Issue 7(2001) Page Start: 500 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗