1. A clinical and genetic study of campomelic dysplasia. Issue 6 (June 1995) Authors: Mansour, S; Hall, C M; Pembrey, M E; Young, I D Journal: Journal of medical genetics Issue: Volume 32:Issue 6(1995) Page Start: 415 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A distinct form of spondyloepimetaphyseal dysplasia with multiple dislocations. Issue 7 (July 1998) Authors: Hall, C M; Elçioglu, N H; Shaw, D G Journal: Journal of medical genetics Issue: Volume 35:Issue 7(1998) Page Start: 566 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A lethal skeletal dysplasia with features of chondrodysplasia punctata and osteogenesis imperfecta: an example of Astley-Kendall dysplasia. Further delineation of a rare genetic disorder. Issue 6 (June 1998) Authors: Elçioglu, N; Hall, C M Journal: Journal of medical genetics Issue: Volume 35:Issue 6(1998) Page Start: 505 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Amiodarone and breast feeding. Issue 3 (1st May 2003) Authors: Hall, C M; McCormick, K P B Journal: Archives of disease in childhood Issue: Volume 88:Issue 3(2003) Page Start: F255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia). Issue 2 (April 1982) Authors: Harding, A E; Hall, C M; Baraitser, M Journal: Journal of medical genetics Issue: Volume 19:Issue 2(1982) Page Start: 110 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cervical spine fractures and rear car seat restraints. Issue 12 (December 1987) Authors: Conry, B G; Hall, C M Journal: Archives of disease in childhood Issue: Volume 62:Issue 12(1987) Page Start: 1267 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes. Issue 12 (18th December 2003) Authors: Oosterwijk, J C; Mansour, S; van Noort, G; Waterham, H R; Hall, C M; Hennekam, R C M Journal: Journal of medical genetics Issue: Volume 40:Issue 12(2003) Page Start: 937 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis. Issue 8 (August 1997) Authors: Reardon, W; Wilkes, D; Rutland, P; Pulleyn, L J; Malcolm, S; Dean, J C; Evans, R D; Jones, B M; Hayward, R; Hall, C M; Nevin, N C; Baraister, M; Winter, R M Journal: Journal of medical genetics Issue: Volume 34:Issue 8(1997) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Current results of surgery for achalasia of the cardia. Issue 6 (June 1993) Authors: Emblem, R; Stringer, M D; Hall, C M; Spitz, L Journal: Archives of disease in childhood Issue: Volume 68:Issue 6(1993) Page Start: 749 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Dilated cardiomyopathy, sudden cardiac death, hypoplastic discs, and retinal detachment: a new autosomal dominant syndrome. Issue 3 (1st March 2002) Authors: Goodship, J A; O'Sullivan, J; Chinnery, P F; Ryan, A K; Ziakas, N; Hall, C M; Clarke, M Journal: Journal of medical genetics Issue: Volume 39:Issue 3(2002) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗