1. Births resulting from assisted conception. Issue 6741 (30th June 1990) Authors: Chitty, L; Pembrey, M Journal: BMJ Issue: Volume 300:Issue 6741(1990) Page Start: 1726 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Congenital cutis laxa with retardation of growth and development. Issue 9 (September 1987) Authors: Patton, M A; Tolmie, J; Ruthnum, P; Bamforth, S; Baraitser, M; Pembrey, M Journal: Journal of medical genetics Issue: Volume 24:Issue 9(1987) Page Start: 556 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Dominantly inherited cleft lip and palate in two families. Issue 6 (June 1989) Authors: Temple, K; Calvert, M; Plint, D; Thompson, E; Pembrey, M Journal: Journal of medical genetics Issue: Volume 26:Issue 6(1989) Page Start: 386 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene. Issue 11 (November 1983) Authors: Mossman, J; Blunt, S; Stephens, R; Jones, E E; Pembrey, M Journal: Archives of disease in childhood Issue: Volume 58:Issue 11(1983) Page Start: 911 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Impact of molecular biology on clinical genetics. Issue 6600 (19th September 1987) Authors: Pembrey, M Journal: BMJ Issue: Volume 295:Issue 6600(1987) Page Start: 711 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Phenotypic variation in LADD syndrome. Issue 5 (October 1985) Authors: Thompson, E; Pembrey, M; Graham, J M Journal: Journal of medical genetics Issue: Volume 22:Issue 5(1985) Page Start: 382 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Prader-Willi Syndrome: Selected Research and Management Issues. Issue 12 (December 1989) Authors: Pembrey, M Journal: Journal of medical genetics Issue: Volume 26:Issue 12(1989) Page Start: 797 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Seckel syndrome: an overdiagnosed syndrome. Issue 3 (June 1985) Authors: Thompson, E; Pembrey, M Journal: Journal of medical genetics Issue: Volume 22:Issue 3(1985) Page Start: 192 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Sickle cell disease in Saudi Arabs in early childhood. Issue 3 (March 1981) Authors: Perrine, R P; John, P; Pembrey, M; Perrine, S Journal: Archives of disease in childhood Issue: Volume 56:Issue 3(1981) Page Start: 187 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The association of Angelman's syndrome with deletions within 15q11-13. Issue 2 (February 1989) Authors: Pembrey, M; Fennell, S J; van den Berghe, J; Fitchett, M; Summers, D; Butler, L; Clarke, C; Griffiths, M; Thompson, E; Super, M Journal: Journal of medical genetics Issue: Volume 26:Issue 2(1989) Page Start: 73 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗