1. Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy. Issue 4 (April 1998) Authors: Speer, M C; Gilchrist, J M; Stajich, J M; Gaskell, P C; Westbrook, C A; Horrigan, S K; Bartoloni, L; Yamaoka, L H; Scott, W K; Pericak-Vance, M A Journal: Journal of medical genetics Issue: Volume 35:Issue 4(1998) Page Start: 305 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B. Issue 10 (October 1995) Authors: Gilbert, J R; Speer, M C; Stajich, J; Clancy, R; Lewis, K; Qiu, H; Yamaoka, L; Kumar, A; Vance, J; Stewart, C; Rozear, M; Roses, A D; Pericak-Vance, M A Journal: Journal of medical genetics Issue: Volume 32:Issue 10(1995) Page Start: 770 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype. Issue 12 (December 1994) Authors: McAllister, K A; Lennon, F; Bowles-Biesecker, B; McKinnon, W C; Helmbold, E A; Markel, D S; Jackson, C E; Guttmacher, A E; Pericak-Vance, M A; Marchuk, D A Journal: Journal of medical genetics Issue: Volume 31:Issue 12(1994) Page Start: 927 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26. Issue 6 (June 1993) Authors: Pericak-Vance, M A; Nunes, K J; Whisenant, E; Loeb, D B; Small, K W; Stajich, J M; Rimmler, J B; Yamaoka, L H; Smith, D I; Drabkin, H A Journal: Journal of medical genetics Issue: Volume 30:Issue 6(1993) Page Start: 487 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer's disease. Issue 10 (30th September 2005) Authors: Martin, E R; Bronson, P G; Li, Y-J; Wall, N; Chung, R-H; Schmechel, D E; Small, G; Xu, P-T; Bartlett, J; Schnetz-Boutaud, N; Haines, J L; Gilbert, J R; Pericak-Vance, M A Journal: Journal of medical genetics Issue: Volume 42:Issue 10(2005) Page Start: 787 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease. Issue 8 (August 1989) Authors: Siddique, T; Roper, H; Pericak-Vance, M A; Shaw, J; Warner, K L; Hung, W Y; Phillips, K L; Lunt, P; Cumming, W J; Roses, A D Journal: Journal of medical genetics Issue: Volume 26:Issue 8(1989) Page Start: 487 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8. Issue 9 (September 1987) Authors: Diehl, S R; Boehnke, M; Collins, F S; Erickson, R P; Karolyi, I J; Ploughman, L M; Pericak-Vance, M A; Aylsworth, A S; Roses, A D Journal: Journal of medical genetics Issue: Volume 24:Issue 9(1987) Page Start: 532 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Linkage studies in peripheral neurofibromatosis. Issue 9 (September 1987) Authors: Pericak-Vance, M A; Yamaoka, L H; Vance, J M; Aylsworth, A S; Rossenwasser, G O; Gaskell, P C; Alberts, M J; Hung, W Y; Haynes, C; Roses, A D Journal: Journal of medical genetics Issue: Volume 24:Issue 9(1987) Page Start: 530 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗