1. A familial syndrome of short stature, deformities of the hands and feet, and an unusual facies. Issue 4 (December 1970) Authors: Emery, A E; Nelson, M M Journal: Journal of medical genetics Issue: Volume 7:Issue 4(1970) Page Start: 379 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A family study of Charcot-Marie-Tooth disease. Issue 2 (April 1982) Authors: Brooks, A P; Emery, A E Journal: Journal of medical genetics Issue: Volume 19:Issue 2(1982) Page Start: 88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A family study of Paget's disease of bone. Issue 3 (September 1983) Authors: Sofaer, J A; Holloway, S M; Emery, A E Journal: Journal of epidemiology and community health Issue: Volume 37:Issue 3(1983) Page Start: 226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A population study of adult onset limb-girdle muscular dystrophy. Issue 4 (August 1985) Authors: Yates, J R; Emery, A E Journal: Journal of medical genetics Issue: Volume 22:Issue 4(1985) Page Start: 250 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party. Issue 6 (December 1978) Authors: Emery, A E; Brough, C; Crawfurd, M; Harper, P; Harris, R; Oakshott, G Journal: Journal of medical genetics Issue: Volume 15:Issue 6(1978) Page Start: 435 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Abnormalities of the electrocardiogram in hereditary myopathies. Issue 1 (March 1972) Authors: Emery, A E Journal: Journal of medical genetics Issue: Volume 9:Issue 1(1972) Page Start: 8 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Apparent enhanced response to the induction of sister chromatid exchange by mitomycin C in myotonic dystrophy. Issue 2 (April 1982) Authors: Vijayalaxmi, ; Emery, A E; Evans, H J Journal: Journal of medical genetics Issue: Volume 19:Issue 2(1982) Page Start: 135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Bloch-Sulzberger Syndrome (incontinentia pigmenti). Issue 2 (June 1966) Authors: Shotts, N; Emery, A E Journal: Journal of medical genetics Issue: Volume 3:Issue 2(1966) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Clinical and chromosome studies in Fanconi's aplastic anaemia. Issue 1 (March 1969) Authors: Perkins, J; Timson, J; Emery, A E Journal: Journal of medical genetics Issue: Volume 6:Issue 1(1969) Page Start: 28 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Detection of carriers of benign X-linked muscular dystrophy. Issue 5578 (2nd December 1967) Authors: Emery, A E; Clack, E R; Simon, S; Taylor, J L Journal: BMJ Issue: Volume 4:Issue 5578(1967) Page Start: 522 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗