1. Exclusion of COL2A1 as a candidate gene in a family with Wagner-Stickler syndrome. Issue 2 (February 1990) Authors: Fryer, A E; Upadhyaya, M; Littler, M; Bacon, P; Watkins, D; Tsipouras, P; Harper, P S Journal: Journal of medical genetics Issue: Volume 27:Issue 2(1990) Page Start: 91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Forehead plaque: a presenting skin sign in tuberous sclerosis. Issue 3 (March 1987) Authors: Fryer, A E; Osborne, J P; Schutt, W Journal: Archives of disease in childhood Issue: Volume 62:Issue 3(1987) Page Start: 292 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl. Issue 9 (September 1987) Authors: Connor, J M; Pirrit, L A; Yates, J R; Fryer, A E; Ferguson-Smith, M A Journal: Journal of medical genetics Issue: Volume 24:Issue 9(1987) Page Start: 544 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. On the incidence of fits and mental retardation in tuberous sclerosis. Issue 6 (June 1991) Authors: Webb, D W; Fryer, A E; Osborne, J P Journal: Journal of medical genetics Issue: Volume 28:Issue 6(1991) Page Start: 395 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Recurrence of orbital cysts in the branchio-oculo-facial syndrome. Issue 6 (June 1992) Authors: Fielding, D W; Fryer, A E Journal: Journal of medical genetics Issue: Volume 29:Issue 6(1992) Page Start: 430 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Recurrence of Pallister-Hall syndrome in two sibs. Issue 2 (February 1994) Authors: Thomas, H M; Todd, P J; Heaf, D; Fryer, A E Journal: Journal of medical genetics Issue: Volume 31:Issue 2(1994) Page Start: 145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study. Issue 3 (14th March 2007) Authors: Quarrell, Oliver W J; Rigby, Alan S; Barron, L; Crow, Y; Dalton, A; Dennis, N; Fryer, A E; Heydon, F; Kinning, E; Lashwood, A; Losekoot, M; Margerison, L; McDonnell, S; Morrison, P J; Norman, A; Peterson, M; Raymond, F L; Simpson, S; Thompson, E; Warner, J Journal: Journal of medical genetics Issue: Volume 44:Issue 3(2007) Page Start: e68 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The value of investigation for genetic counselling in tuberous sclerosis. Issue 4 (April 1990) Authors: Fryer, A E; Chalmers, A H; Osborne, J P Journal: Journal of medical genetics Issue: Volume 27:Issue 4(1990) Page Start: 217 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Tuberous sclerosis: a large family with no history of seizures or mental retardation. Issue 9 (September 1987) Authors: Fryer, A E; Osborne, J P; Tan, R; Siggers, D C Journal: Journal of medical genetics Issue: Volume 24:Issue 9(1987) Page Start: 547 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗