1. A case of Fryns syndrome. Issue 1 (February 1986) Authors: Young, I D; Simpson, K; Winter, R M Journal: Journal of medical genetics Issue: Volume 23:Issue 1(1986) Page Start: 82 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A combinatorial method for grouping cases with multiple malformations. Issue 2 (February 1988) Authors: Winter, R M; Clark, R D; Ashley, K; Gibbs, G Journal: Journal of medical genetics Issue: Volume 25:Issue 2(1988) Page Start: 118 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A computerised data base for the diagnosis of rare dysmorphic syndromes. Issue 2 (April 1984) Authors: Winter, R M; Baraitser, M; Douglas, J M Journal: Journal of medical genetics Issue: Volume 21:Issue 2(1984) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A diagnostic survey of infants referred for chromosome analysis in the neonatal period. Issue 6247 (18th October 1980) Authors: Winter, R M; Ridler, M A; McKeown, J A Journal: BMJ Issue: Volume 281:Issue 6247(1980) Page Start: 1045 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A lethal short rib syndrome without polydactyly. Issue 5 (May 1988) Authors: Winter, R M Journal: Journal of medical genetics Issue: Volume 25:Issue 5(1988) Page Start: 349 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A male infant with the Catel-Manzke syndrome and dislocatable knees. Issue 3 (June 1986) Authors: Thompson, E M; Winter, R M; Williams, M J Journal: Journal of medical genetics Issue: Volume 23:Issue 3(1986) Page Start: 271 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A new type of osteogenesis imperfecta. Issue 2 (April 1982) Authors: Crawfurd, M D; Winter, R M Journal: Journal of medical genetics Issue: Volume 19:Issue 2(1982) Page Start: 158 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A possible human homologue for the mouse mutant disorganisation. Issue 7 (July 1989) Authors: Winter, R M; Donnai, D Journal: Journal of medical genetics Issue: Volume 26:Issue 7(1989) Page Start: 417 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A previously undescribed syndrome of thoracic dysplasia and communicating hydrocephalus in two sibs, one diagnosed prenatally by ultrasound. Issue 4 (April 1987) Authors: Winter, R M; Campbell, S; Wigglesworth, J S; Nevrkla, E J Journal: Journal of medical genetics Issue: Volume 24:Issue 4(1987) Page Start: 204 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A recognisable short stature syndrome with premature aging and pigmented naevi. Issue 1 (January 1988) Authors: Baraitser, M; Insley, J; Winter, R M Journal: Journal of medical genetics Issue: Volume 25:Issue 1(1988) Page Start: 53 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗