1. A family study of hidradenitis suppurativa. Issue 5 (October 1985) Authors: Fitzsimmons, J S; Guilbert, P R Journal: Journal of medical genetics Issue: Volume 22:Issue 5(1985) Page Start: 367 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Antenatal diagnosis of trisomy 13 with unexpected increase in alpha-feto protein. Issue 5 (October 1976) Authors: Fitzsimmons, J S; Filshie, G M; Hill, A S; Kime, R Journal: Journal of medical genetics Issue: Volume 13:Issue 5(1976) Page Start: 400 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Carrier detection in Duchenne muscular dystrophy. Issue 3 (June 1980) Authors: Fitzsimmons, J S; McLachlan, J I; Reeves, W G; Marriott, D W; Woolfson, A M; Mayhew, J Journal: Journal of medical genetics Issue: Volume 17:Issue 3(1980) Page Start: 165 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Classroom teaching in genetics and birth defects: the Nottingham experience. Issue 5 (October 1985) Authors: Fitzsimmons, J S Journal: Journal of medical genetics Issue: Volume 22:Issue 5(1985) Page Start: 345 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Congenital discoid lupus in the newborn. Issue 4 (August 1977) Authors: Fitzsimmons, J S; Crawford, M J; Reeves, W G Journal: Journal of medical genetics Issue: Volume 14:Issue 4(1977) Page Start: 283 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cutis marmorata telangiectatica congenita or congenital generalized phlebectasia. Issue 243 (October 1970) Authors: Fitzsimmons, J S; Starks, M Journal: Archives of disease in childhood Issue: Volume 45:Issue 243(1970) Page Start: 724 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Familial hidradenitis suppurativa: evidence in favour of single gene transmission. Issue 4 (August 1984) Authors: Fitzsimmons, J S; Fitzsimmons, E M; Gilbert, G Journal: Journal of medical genetics Issue: Volume 21:Issue 4(1984) Page Start: 281 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Familial spastic paraplegia, bilateral sensorineural deafness, and intellectual retardation associated with a progressive nephropathy. Issue 3 (March 1988) Authors: Fitzsimmons, J S; Watson, A R; Mellor, D; Guilbert, P R Journal: Journal of medical genetics Issue: Volume 25:Issue 3(1988) Page Start: 168 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genetic heterogeneity in the Freeman-Sheldon syndrome: two adults with probable autosomal recessive inheritance. Issue 5 (October 1984) Authors: Fitzsimmons, J S; Zaldua, V; Chrispin, A R Journal: Journal of medical genetics Issue: Volume 21:Issue 5(1984) Page Start: 364 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Letter: Serum alpha-fetoprotein in cystic fibrosis. Issue 5982 (30th August 1975) Authors: Fitzsimmons, J S; Smith, N; Hiller, E J; Wynne, J Journal: BMJ Issue: Volume 3:Issue 5982(1975) Page Start: 544 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗