1. A register based system for gene tracking in Duchenne muscular dystrophy. Issue 6 (December 1986) Authors: Read, A P; Kerzin-Storrar, L; Mountford, R C; Elles, R G; Harris, R Journal: Journal of medical genetics Issue: Volume 23:Issue 6(1986) Page Start: 581 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Apparent prevention of neural tube defects by periconceptional vitamin supplementation. Issue 12 (December 1981) Authors: Smithells, R W; Sheppard, S; Schorah, C J; Seller, M J; Nevin, N C; Harris, R; Read, A P; Fielding, D W Journal: Archives of disease in childhood Issue: Volume 56:Issue 12(1981) Page Start: 911 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Beckwith-Wiedemann syndrome. Issue 9 (September 1992) Authors: Norman, A M; Read, A P; Donnai, D Journal: Journal of medical genetics Issue: Volume 29:Issue 9(1992) Page Start: 679 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Bridging markers defining the map position of X linked hypophosphataemic rickets. Issue 12 (December 1987) Authors: Thakker, R V; Read, A P; Davies, K E; Whyte, M P; Weksberg, R; Glorieux, F; Davies, M; Mountford, R C; Harris, R; King, A Journal: Journal of medical genetics Issue: Volume 24:Issue 12(1987) Page Start: 756 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q. Issue 7 (July 1995) Authors: Van Camp, G; Van Thienen, M N; Handig, I; Van Roy, B; Rao, V S; Milunsky, A; Read, A P; Baldwin, C T; Farrer, L A; Bonduelle, M Journal: Journal of medical genetics Issue: Volume 32:Issue 7(1995) Page Start: 531 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cloning for gold. Issue 3 (September 1997) Authors: Read, A P Journal: British journal of sports medicine Issue: Volume 31:Issue 3(1997) Page Start: 174 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Consanguinity and complex cardiac anomalies with situs ambiguus. Issue 3 (March 1984) Authors: Gatrad, A R; Read, A P; Watson, G H Journal: Archives of disease in childhood Issue: Volume 59:Issue 3(1984) Page Start: 242 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Costs and benefits of serum alpha-fetoprotein screening. Issue 6154 (23rd December 1978) Authors: Read, A P Journal: BMJ Issue: Volume 2:Issue 6154(1978) Page Start: 1787 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Diagnosis of adult polycystic kidney disease by genetic markers and ultrasonographic imaging in a voluntary family register. Issue 2 (February 1994) Authors: Elles, R G; Hodgkinson, K A; Mallick, N P; O'Donoghue, D J; Read, A P; Rimmer, S; Watters, E A; Harris, R Journal: Journal of medical genetics Issue: Volume 31:Issue 2(1994) Page Start: 115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomas. Issue 12 (December 1998) Authors: Wu, C L; Thakker, N; Neary, W; Black, G; Lye, R; Ramsden, R T; Read, A P; Evans, D G Journal: Journal of medical genetics Issue: Volume 35:Issue 12(1998) Page Start: 973 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗