1. A clinical study of type 1 neurofibromatosis in north west England. Issue 3 (1st March 1999) Authors: McGaughran, J M; Harris, D I; Donnai, D; Teare, D; MacLeod, R; Westerbeek, R; Kingston, H; Super, M; Harris, R; Evans, D G R Journal: Journal of medical genetics Issue: Volume 36:Issue 3(1999) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A further case of a new syndrome including midface retraction, hypertrichosis, and skeletal anomalies. Issue 6 (December 1979) Authors: Donnai, D; Harris, R Journal: Journal of medical genetics Issue: Volume 16:Issue 6(1979) Page Start: 483 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A further patient with the lethal type of Larsen syndrome. Issue 7 (July 1988) Authors: Clayton-Smith, J; Donnai, D Journal: Journal of medical genetics Issue: Volume 25:Issue 7(1988) Page Start: 499 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity. Issue 12 (December 1992) Authors: Evans, D G; Huson, S M; Donnai, D; Neary, W; Blair, V; Teare, D; Newton, V; Strachan, T; Ramsden, R; Harris, R Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 841 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counselling. Issue 12 (December 1992) Authors: Evans, D G; Huson, S M; Donnai, D; Neary, W; Blair, V; Newton, V; Strachan, T; Harris, R Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 847 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A new recessive syndrome of unusual facies and multiple structural abnormalities. Issue 9 (September 1991) Authors: Thakker, Y; Donnai, D Journal: Journal of medical genetics Issue: Volume 28:Issue 9(1991) Page Start: 633 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis. Issue 5 (May 1989) Authors: Clayton-Smith, J; Donnai, D Journal: Journal of medical genetics Issue: Volume 26:Issue 5(1989) Page Start: 339 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A possible human homologue for the mouse mutant disorganisation. Issue 7 (July 1989) Authors: Winter, R M; Donnai, D Journal: Journal of medical genetics Issue: Volume 26:Issue 7(1989) Page Start: 417 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Ankyloblepharon filiforme adnatum in trisomy 18 Edwards syndrome. Issue 11 (November 1990) Authors: Evans, D G; Evans, I D; Donnai, D; Lindenbaum, R H Journal: Journal of medical genetics Issue: Volume 27:Issue 11(1990) Page Start: 720 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Anorectal malformation: familial aspects and associated anomalies. Issue 6 (June 1987) Authors: Boocock, G R; Donnai, D Journal: Archives of disease in childhood Issue: Volume 62:Issue 6(1987) Page Start: 576 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗