1. Apple peel syndrome in sibs. Issue 1 (January 1989) Authors: Farag, T I; Teebi, A S Journal: Journal of medical genetics Issue: Volume 26:Issue 1(1989) Page Start: 67 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Autosomal dominant sneezing disorder provoked by fullness of stomach. Issue 8 (August 1989) Authors: Teebi, A S; al-Saleh, Q A Journal: Journal of medical genetics Issue: Volume 26:Issue 8(1989) Page Start: 539 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Autosomal recessive disorders among Arabs: an overview from Kuwait. Issue 3 (March 1994) Authors: Teebi, A S Journal: Journal of medical genetics Issue: Volume 31:Issue 3(1994) Page Start: 224 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autosomal recessive epidermolytic palmoplantar keratoderma. Issue 8 (August 1990) Authors: Alsaleh, Q A; Teebi, A S Journal: Journal of medical genetics Issue: Volume 27:Issue 8(1990) Page Start: 519 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Brachmann-de Lange syndrome in sibs. Issue 10 (October 1987) Authors: Naguib, K K; Teebi, A S; Al-Awadi, S A; Marafie, M J Journal: Journal of medical genetics Issue: Volume 24:Issue 10(1987) Page Start: 627 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23----q25. Issue 1 (February 1986) Authors: Al-Awadi, S A; Naguib, K K; Farag, T I; Teebi, A S; Cuschieri, A; Al-Othman, S A; Sundareshan, T S Journal: Journal of medical genetics Issue: Volume 23:Issue 1(1986) Page Start: 91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Craniofacial anomalies, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation in two sisters: a new autosomal recessive MCA/MR syndrome?. Issue 2 (1st February 2002) Authors: Siegel-Bartlet, J; Levin, A; Teebi, A S; Kennedy, S J Journal: Journal of medical genetics Issue: Volume 39:Issue 2(2002) Page Start: 145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genetic referrals of Middle Eastern origin in a western city: inbreeding and disease profile. Issue 3 (March 1996) Authors: Hoodfar, E; Teebi, A S Journal: Journal of medical genetics Issue: Volume 33:Issue 3(1996) Page Start: 212 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Hypoplastic tibiae with postaxial polysyndactyly: a new dominant syndrome?. Issue 6 (June 1987) Authors: Al-Awadi, S A; Naguib, K K; Farag, T I; Teebi, A S Journal: Journal of medical genetics Issue: Volume 24:Issue 6(1987) Page Start: 369 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Kuwait type faciodigitogenital syndrome. Issue 11 (November 1991) Authors: Teebi, A S; al Awadi, S A Journal: Journal of medical genetics Issue: Volume 28:Issue 11(1991) Page Start: 805 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗