11. A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans. Issue 9 (September 1996) Authors: Wilkes, D; Rutland, P; Pulleyn, L J; Reardon, W; Moss, C; Ellis, J P; Winter, R M; Malcolm, S Journal: Journal of medical genetics Issue: Volume 33:Issue 9(1996) Page Start: 744 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Advances in genetics. Issue 4 (October 1996) Authors: Lees, M M; Winter, R M Journal: Archives of disease in childhood Issue: Volume 75:Issue 4(1996) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Alagille syndrome: family studies. Issue 4 (April 1995) Authors: Elmslie, F V; Vivian, A J; Gardiner, H; Hall, C; Mowat, A P; Winter, R M Journal: Journal of medical genetics Issue: Volume 32:Issue 4(1995) Page Start: 264 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. An Introduction to Recombinant DNA. Issue 2 (February 1985) Authors: Winter, R M Journal: Archives of disease in childhood Issue: Volume 60:Issue 2(1985) Page Start: 190 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Another family with the 'Habsburg jaw'. Issue 12 (December 1988) Authors: Thompson, E M; Winter, R M Journal: Journal of medical genetics Issue: Volume 25:Issue 12(1988) Page Start: 838 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Apparent microcephaly caused by a bicornuate uterus. Issue 6378 (21st May 1983) Authors: Winter, R M; Dearlove, J; Jolly, H; Pawson, M; Wilson, R G Journal: BMJ Issue: Volume 286:Issue 6378(1983) Page Start: 1640 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia. Issue 6 (June 1991) Authors: Brunner, H G; Winter, R M Journal: Journal of medical genetics Issue: Volume 28:Issue 6(1991) Page Start: 389 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Clinical studies on submicroscopic subtelomeric rearrangements: a checklist. Issue 3 (1st March 2001) Authors: de Vries, B B A; White, S M; Knight, S J L; Regan, R; Homfray, T; Young, I D; Super, M; McKeown, C; Splitt, M; Quarrell, O W J; Trainer, A H; Niermeijer, M F; Malcolm, S; Flint, J; Hurst, J A; Winter, R M Journal: Journal of medical genetics Issue: Volume 38:Issue 3(2001) Page Start: 145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy. Issue 3 (March 1984) Authors: Pembrey, M E; Davies, K E; Winter, R M; Elles, R G; Williamson, R; Fazzone, T A; Walker, C Journal: Archives of disease in childhood Issue: Volume 59:Issue 3(1984) Page Start: 208 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate. Issue 6 (June 1992) Authors: Holder, S E; Vintiner, G M; Farren, B; Malcolm, S; Winter, R M Journal: Journal of medical genetics Issue: Volume 29:Issue 6(1992) Page Start: 390 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗