1. A syndrome of insulin resistance resembling leprechaunism in five sibs of consanguineous parents. Issue 6 (June 1993) Authors: al-Gazali, L I; Khalil, M; Devadas, K Journal: Journal of medical genetics Issue: Volume 30:Issue 6(1993) Page Start: 470 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?. Issue 9 (September 1992) Authors: Revesz, T; Fletcher, S; al-Gazali, L I; DeBuse, P Journal: Journal of medical genetics Issue: Volume 29:Issue 9(1992) Page Start: 673 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosis. Issue 11 (November 1989) Authors: al-Gazali, L I; Arthur, R J; Lamb, J T; Hammer, H M; Coker, T P; Hirschmann, P N; Gibbs, J; Mueller, R F Journal: Journal of medical genetics Issue: Volume 26:Issue 11(1989) Page Start: 694 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Further delineation of Nevo syndrome. Issue 5 (May 1997) Authors: al-Gazali, L I; Bakalinova, D; Varady, E; Scorer, J; Nork, M Journal: Journal of medical genetics Issue: Volume 34:Issue 5(1997) Page Start: 366 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1. Issue 8 (August 1997) Authors: Brown, K A; al-Gazali, L I; Moynihan, L M; Lench, N J; Markham, A F; Mueller, R F Journal: Journal of medical genetics Issue: Volume 34:Issue 8(1997) Page Start: 685 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features: a distinct autosomal recessive syndrome?. Issue 11 (November 1988) Authors: al-Gazali, L I; Donnai, D; Mueller, R F Journal: Journal of medical genetics Issue: Volume 25:Issue 11(1988) Page Start: 758 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Homozygosity for a new mutation (Ile119-->Met) in the insulin receptor gene in five sibs with familial insulin resistance. Issue 9 (September 1994) Authors: Hone, J; Accili, D; al-Gazali, L I; Lestringant, G; Orban, T; Taylor, S I Journal: Journal of medical genetics Issue: Volume 31:Issue 9(1994) Page Start: 715 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The oculocerebrocutaneous (Delleman) syndrome. Issue 11 (November 1988) Authors: al-Gazali, L I; Donnai, D; Berry, S A; Say, B; Mueller, R F Journal: Journal of medical genetics Issue: Volume 25:Issue 11(1988) Page Start: 773 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The profile of major congenital abnormalities in the United Arab Emirates (UAE) population. Issue 1 (January 1995) Authors: al-Gazali, L I; Dawodu, A H; Sabarinathan, K; Varghese, M Journal: Journal of medical genetics Issue: Volume 32:Issue 1(1995) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The Schinzel-Giedion syndrome. Issue 1 (January 1990) Authors: al-Gazali, L I; Farndon, P; Burn, J; Flannery, D B; Davison, C; Mueller, R F Journal: Journal of medical genetics Issue: Volume 27:Issue 1(1990) Page Start: 42 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗