1. A Scottish family with Bazex-Dupré-Christol syndrome: follicular atrophoderma, congenital hypotrichosis, and basal cell carcinoma. Issue 6 (June 1996) Authors: Kidd, A; Carson, L; Gregory, D W; de Silva, D; Holmes, J; Dean, J C; Haites, N Journal: Journal of medical genetics Issue: Volume 33:Issue 6(1996) Page Start: 493 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Ascertainment of myotonic dystrophy through cataract by selective screening. Issue 7 (July 1995) Authors: Kidd, A; Turnpenny, P; Kelly, K; Clark, C; Church, W; Hutchinson, C; Dean, J C; Haites, N E Journal: Journal of medical genetics Issue: Volume 32:Issue 7(1995) Page Start: 519 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cardiofaciocutaneous syndrome with new ectodermal manifestations. Issue 6 (June 1992) Authors: Turnpenny, P D; Dean, J C; Auchterlonie, I A; Johnston, A W Journal: Journal of medical genetics Issue: Volume 29:Issue 6(1992) Page Start: 428 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Counselling pitfalls in Romano-Ward syndrome. Issue 10 (October 1993) Authors: Dean, J C; Cross, S; Jennings, K Journal: Journal of medical genetics Issue: Volume 30:Issue 10(1993) Page Start: 886 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cranial hemihypertrophy and neurodevelopmental prognosis. Issue 3 (March 1990) Authors: Dean, J C; Cole, G F; Appleton, R E; Burn, J; Roberts, S A; Donnai, D Journal: Journal of medical genetics Issue: Volume 27:Issue 3(1990) Page Start: 160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Craniosynostosis and chromosome 22q11 deletion. Issue 4 (April 1998) Authors: Dean, J C; De Silva, D C; Reardon, W Journal: Journal of medical genetics Issue: Volume 35:Issue 4(1998) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis. Issue 8 (August 1997) Authors: Reardon, W; Wilkes, D; Rutland, P; Pulleyn, L J; Malcolm, S; Dean, J C; Evans, R D; Jones, B M; Hayward, R; Hall, C M; Nevin, N C; Baraister, M; Winter, R M Journal: Journal of medical genetics Issue: Volume 34:Issue 8(1997) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Evidence of genetic and phenotypic heterogeneity in the Romano-Ward syndrome. Issue 11 (November 1993) Authors: Dean, J C; Cross, S; Jennings, K Journal: Journal of medical genetics Issue: Volume 30:Issue 11(1993) Page Start: 947 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Facial dysmorphism: a marker of autosomal dominant cranial diabetes insipidus. Issue 8 (August 1991) Authors: Laing, R B; Dean, J C; Pearson, D W; Johnston, A W Journal: Journal of medical genetics Issue: Volume 28:Issue 8(1991) Page Start: 544 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Interstitial deletion of chromosome 13: prognosis and adult phenotype. Issue 8 (August 1991) Authors: Dean, J C; Simpson, S; Couzin, D A; Stephen, G S Journal: Journal of medical genetics Issue: Volume 28:Issue 8(1991) Page Start: 533 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗