1. DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin. Issue 4 (October 1991) Authors: Wilson, D I; Cross, I E; Goodship, J A; Coulthard, S; Carey, A H; Scambler, P J; Bain, H H; Hunter, A S; Carter, P E; Burn, J Journal: Heart Issue: Volume 66:Issue 4(1991) Page Start: 308 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. DiGeorge syndrome: part of CATCH 22. Issue 10 (October 1993) Authors: Wilson, D I; Burn, J; Scambler, P; Goodship, J Journal: Journal of medical genetics Issue: Volume 30:Issue 10(1993) Page Start: 852 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Fetal and infantile hypertension caused by unilateral renal arterial disease. Issue 8 (August 1990) Authors: Wilson, D I; Appleton, R E; Coulthard, M G; Lee, R E; Wren, C; Bain, H H Journal: Archives of disease in childhood Issue: Volume 65:Issue 8(1990) Page Start: 881 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype. Issue 9 (1st September 2000) Authors: Jones, E A; Clement-Jones, M; Wilson, D I Journal: Journal of medical genetics Issue: Volume 37:Issue 9(2000) Page Start: 658 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Noonan's and DiGeorge syndromes with monosomy 22q11. Issue 2 (February 1993) Authors: Wilson, D I; Britton, S B; McKeown, C; Kelly, D; Cross, I E; Strobel, S; Scambler, P J Journal: Archives of disease in childhood Issue: Volume 68:Issue 2(1993) Page Start: 187 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Reply to letters regarding clinical features of chromosome 22q11 deletion. Issue 4 (April 1998) Authors: Ryan, A; Goodship, J A; Wilson, D I Journal: Journal of medical genetics Issue: Volume 35:Issue 4(1998) Page Start: 347 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. Issue 10 (October 1997) Authors: Ryan, A K; Goodship, J A; Wilson, D I; Philip, N; Levy, A; Seidel, H; Schuffenhauer, S; Oechsler, H; Belohradsky, B; Prieur, M; Aurias, A; Raymond, F L; Clayton-Smith, J; Hatchwell, E; McKeown, C; Beemer, F A; Dallapiccola, B; Novelli, G; Hurst, J A; Ignatius, J Journal: Journal of medical genetics Issue: Volume 34:Issue 10(1997) Page Start: 798 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3. Issue 9 (5th September 2003) Authors: Brickwood, S; Bonthron, D T; Al-Gazali, L I; Piper, K; Hearn, T; Wilson, D I; Hanley, N A Journal: Journal of medical genetics Issue: Volume 40:Issue 9(2003) Page Start: 685 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗