1. A new recognisable syndrome in three sibs with congenital heart disease, round face with depressed nasal bridge, short stature, and developmental retardation. Issue 10 (October 1988) Authors: Sonoda, T; Ohdo, S; Madokoro, H; Ohba, K Journal: Journal of medical genetics Issue: Volume 25:Issue 10(1988) Page Start: 711 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Association of ectodermal dysplasia, ectrodactyly, and macular dystrophy: the EEM syndrome. Issue 1 (February 1983) Authors: Ohdo, S; Hirayama, K; Terawaki, T Journal: Journal of medical genetics Issue: Volume 20:Issue 1(1983) Page Start: 52 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation. Issue 10 (October 1987) Authors: Ohdo, S; Madokoro, H; Sonoda, T; Takei, M; Yasuda, H; Mori, N Journal: Journal of medical genetics Issue: Volume 24:Issue 10(1987) Page Start: 609 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Distal symphalangism associated with camptodactyly. Issue 6 (December 1981) Authors: Ohdo, S; Yamauchi, Y; Hayakawa, K Journal: Journal of medical genetics Issue: Volume 18:Issue 6(1981) Page Start: 456 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Interstitial deletion of the long arm of chromosome 5: 46, XX, del(5)(q13q22). Issue 6 (December 1982) Authors: Ohdo, S; Madokoro, H; Hayakawa, K Journal: Journal of medical genetics Issue: Volume 19:Issue 6(1982) Page Start: 479 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Kabuki make-up syndrome (Niikawa-Kuroki syndrome) associated with congenital heart disease. Issue 2 (April 1985) Authors: Ohdo, S; Madokoro, H; Sonoda, T; Nishiguchi, T; Kawaguchi, K; Hayakawa, K Journal: Journal of medical genetics Issue: Volume 22:Issue 2(1985) Page Start: 126 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mental retardation associated with congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth. Issue 3 (June 1986) Authors: Ohdo, S; Madokoro, H; Sonoda, T; Hayakawa, K Journal: Journal of medical genetics Issue: Volume 23:Issue 3(1986) Page Start: 242 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Natural history and postmortem anatomy of a patient with tetra-amelia, ectodermal dysplasia, peculiar face, and developmental retardation (MIM 273390). Issue 12 (December 1994) Authors: Ohdo, S; Sonoda, T; Ohba, K Journal: Journal of medical genetics Issue: Volume 31:Issue 12(1994) Page Start: 980 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Sibs lacking characteristic features of duplication of distal 17q. Issue 7 (July 1989) Authors: Ohdo, S; Madokoro, H; Sonoda, T; Ohba, K Journal: Journal of medical genetics Issue: Volume 26:Issue 7(1989) Page Start: 465 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Trisomy 10p syndrome owing to maternal pericentric inversion. Issue 4 (April 1990) Authors: Ohba, K; Ohdo, S; Sonoda, T Journal: Journal of medical genetics Issue: Volume 27:Issue 4(1990) Page Start: 264 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗