1. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. Issue 7 (1st July 2002) Authors: Brice, G; Mansour, S; Bell, R; Collin, J R O; Child, A H; Brady, A F; Sarfarazi, M; Burnand, K G; Jeffery, S; Mortimer, P; Murday, V A Journal: Journal of medical genetics Issue: Volume 39:Issue 7(2002) Page Start: 478 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Feasibility of family based screening for colorectal neoplasia: experience in one general surgical practice. Issue 1 (January 1993) Authors: Stephenson, B M; Murday, V A; Finan, P J; Quirke, P; Dixon, M F; Bishop, D T Journal: Gut Issue: Volume 34:Issue 1(1993) Page Start: 96 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Germline PTEN mutations in Cowden syndrome-like families. Issue 11 (November 1998) Authors: Marsh, D J; Dahia, P L; Caron, S; Kum, J B; Frayling, I M; Tomlinson, I P; Hughes, K S; Eeles, R A; Hodgson, S V; Murday, V A; Houlston, R; Eng, C Journal: Journal of medical genetics Issue: Volume 35:Issue 11(1998) Page Start: 881 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Muir-Torre syndrome: a variant of the cancer family syndrome. Issue 8 (August 1994) Authors: Hall, N R; Williams, M A; Murday, V A; Newton, J A; Bishop, D T Journal: Journal of medical genetics Issue: Volume 31:Issue 8(1994) Page Start: 627 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗