1. Adoption, genetic disease, and DNA. Issue 4 (October 1993) Authors: Turnpenny, P D; Simpson, S A; McWhinnie, A M Journal: Archives of disease in childhood Issue: Volume 69:Issue 4(1993) Page Start: 411 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cardiofaciocutaneous syndrome with new ectodermal manifestations. Issue 6 (June 1992) Authors: Turnpenny, P D; Dean, J C; Auchterlonie, I A; Johnston, A W Journal: Journal of medical genetics Issue: Volume 29:Issue 6(1992) Page Start: 428 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Diagnosis of non-immune hydrops in the newborn. Issue 1 (July 1994) Authors: Turnpenny, P D Journal: Archives of disease in childhood Issue: Volume 71:Issue 1(1994) Page Start: F71 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evidence for variable gene expression in a large inbred kindred with autosomal recessive spondylocostal dysostosis. Issue 1 (January 1991) Authors: Turnpenny, P D; Thwaites, R J; Boulos, F N Journal: Journal of medical genetics Issue: Volume 28:Issue 1(1991) Page Start: 27 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Ketamine in severe acute asthma. Issue 4 (December 1991) Authors: Turnpenny, P D; Nash, S F Journal: Emergency medicine journal Issue: Volume 8:Issue 4(1991) Page Start: 291 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Kyphomelic dysplasia: the first 10 cases. Issue 4 (April 1990) Authors: Turnpenny, P D; Dakwar, R A; Boulos, F N Journal: Journal of medical genetics Issue: Volume 27:Issue 4(1990) Page Start: 269 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Long term health and neurodevelopment in children exposed to antiepileptic drugs before birth. Issue 4 (1st April 2002) Authors: Dean, J C S; Hailey, H; Moore, S J; Lloyd, D J; Turnpenny, P D; Little, J Journal: Journal of medical genetics Issue: Volume 39:Issue 4(2002) Page Start: 251 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis. Issue 5 (1st May 2003) Authors: Turnpenny, P D; Whittock, N; Duncan, J; Dunwoodie, S; Kusumi, K; Ellard, S Journal: Journal of medical genetics Issue: Volume 40:Issue 5(2003) Page Start: 333 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defects. Issue 9 (September 1992) Authors: Turnpenny, P D; Dean, J C; Duffty, P; Reid, J A; Carter, P Journal: Journal of medical genetics Issue: Volume 29:Issue 9(1992) Page Start: 659 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗