1. 07 Defective mitochondrial mRNA maturation is associated with spastic ataxia. Issue 3 (15th February 2011) Authors: Christos, Proukakis; Patel, H; Chioza, B A; Dick, K; Al-Memar, A; Chrzanowksa-Lightowlers, Z M A; Cross, H; Patton, M A; Lightowlers, R N; Crosby, A H Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 82:Issue 3(2011) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism. Issue 5 (May 1989) Authors: Edwards, B D; Patton, M A; Dilly, S A; Eastwood, J B Journal: Journal of medical genetics Issue: Volume 26:Issue 5(1989) Page Start: 289 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A Noonan-like short stature syndrome with sparse hair. Issue 2 (April 1986) Authors: Baraitser, M; Patton, M A Journal: Journal of medical genetics Issue: Volume 23:Issue 2(1986) Page Start: 161 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus. Issue 3 (March 1992) Authors: Sharland, M; Taylor, R; Patton, M A; Jeffery, S Journal: Journal of medical genetics Issue: Volume 29:Issue 3(1992) Page Start: 188 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findings. Issue 2 (February 1987) Authors: Patton, M A; Baraitser, M; Heagerty, A H; Eady, R A Journal: Journal of medical genetics Issue: Volume 24:Issue 2(1987) Page Start: 118 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations. Issue 1 (January 1992) Authors: Sharland, M; Bleach, N R; Goberdhan, P D; Patton, M A Journal: Journal of medical genetics Issue: Volume 29:Issue 1(1992) Page Start: 50 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Brachydactyly type C associated with shortening of the hallux. Issue 5 (May 1992) Authors: Rowe-Jones, J M; Moss, A L; Patton, M A Journal: Journal of medical genetics Issue: Volume 29:Issue 5(1992) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Congenital cutis laxa with retardation of growth and development. Issue 9 (September 1987) Authors: Patton, M A; Tolmie, J; Ruthnum, P; Bamforth, S; Baraitser, M; Pembrey, M Journal: Journal of medical genetics Issue: Volume 24:Issue 9(1987) Page Start: 556 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Congenital intestinal pseudo-obstruction associated with a giant platelet disorder. Issue 7 (July 1991) Authors: Pollock, I; Holmes, S J K; Patton, M A; Hamilton, P A; Stacey, T E Journal: Journal of medical genetics Issue: Volume 28:Issue 7(1991) Page Start: 495 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Congenital nystagmus cosegregating with a balanced 7;15 translocation. Issue 6 (June 1993) Authors: Patton, M A; Jeffery, S; Lee, N; Hogg, C Journal: Journal of medical genetics Issue: Volume 30:Issue 6(1993) Page Start: 526 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗