1. A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation. Issue 3 (March 1998) Authors: Ghaffari, S R; Boyd, E; Tolmie, J L; Crow, Y J; Trainer, A H; Connor, J M Journal: Journal of medical genetics Issue: Volume 35:Issue 3(1998) Page Start: 225 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of the origin of Turner's syndrome using polymorphic DNA probes. Issue 3 (March 1991) Authors: Loughlin, S A; Redha, A; McIver, J; Boyd, E; Carothers, A; Connor, J M Journal: Journal of medical genetics Issue: Volume 28:Issue 3(1991) Page Start: 156 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Appropriate statistical test in comparative ulcer healing studies. Issue 6 (June 1985) Authors: Boyd, E; Marks, I N Journal: Gut Issue: Volume 26:Issue 6(1985) Page Start: 643 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Children with duodenal ulcers and their families. Issue 6 (June 1975) Authors: Puri, P; Boyd, E Journal: Archives of disease in childhood Issue: Volume 50:Issue 6(1975) Page Start: 485 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis. Issue 2 (February 1987) Authors: Cooke, A; Tolmie, J; Darlington, W; Boyd, E; Thomson, R; Ferguson-Smith, M A Journal: Journal of medical genetics Issue: Volume 24:Issue 2(1987) Page Start: 88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Effect of COVID-19 pandemic lockdowns on planned cancer surgery for 15 tumour types in 61 countries: an international, prospective, cohort study. Issue 11 (November 2021) Authors: Glasbey, James; Ademuyiwa, Adesoji; Adisa, Adewale; AlAmeer, Ehab; Arnaud, Alexis P; Ayasra, Faris; Azevedo, José; Minaya-Bravo, Ana; Costas-Chavarri, Ainhoa; Edwards, John; Elhadi, Muhammed; Fiore, Marco; Fotopoulou, Christina; Gallo, Gaetano; Ghosh, Dhruva; Griffiths, Ewen A; Harrison, Ewen; H... Journal: Lancet oncology Issue: Volume 22:Issue 11(2021) Page Start: 1507 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study. Issue 3 (March 1996) Authors: Reid, E; Morrison, N; Barron, L; Boyd, E; Cooke, A; Fielding, D; Tolmie, J L Journal: Journal of medical genetics Issue: Volume 33:Issue 3(1996) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase. Issue 2 (February 1989) Authors: Glass, I A; Swindlehurst, C A; Aitken, D A; McCrea, W; Boyd, E Journal: Journal of medical genetics Issue: Volume 26:Issue 2(1989) Page Start: 127 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Inv dup (15) with mental retardation but few dysmorphic features. Issue 3 (June 1984) Authors: Gilmore, D H; Boyd, E; McClure, J P; Batstone, P; Connor, J M Journal: Journal of medical genetics Issue: Volume 21:Issue 3(1984) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45, X-46, XYqi). Issue 4 (December 1969) Authors: Ferguson-Smith, M A; Boyd, E; Ferguson-Smith, M E; Pritchard, J G; Yusuf, A F; Gray, B Journal: Journal of medical genetics Issue: Volume 6:Issue 4(1969) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗