11. A terminal deletion of the long arm of chromosome 4 [46, XX, del(4)(q33)] in an infant with phenotypic features of Williams syndrome. Issue 5 (October 1986) Authors: Jefferson, R D; Burn, J; Gaunt, K L; Hunter, S; Davison, E V Journal: Journal of medical genetics Issue: Volume 23:Issue 5(1986) Page Start: 474 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Alagille syndrome and deletion of 20p. Issue 12 (December 1990) Authors: Anad, F; Burn, J; Matthews, D; Cross, I; Davison, B C; Mueller, R; Sands, M; Lillington, D M; Eastham, E Journal: Journal of medical genetics Issue: Volume 27:Issue 12(1990) Page Start: 729 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. An avoidable recurrence of cri du chat syndrome in the next generation. Issue 6401 (29th October 1983) Authors: Burn, J; Baraitser, M; Butler, L J Journal: BMJ Issue: Volume 287:Issue 6401(1983) Page Start: 1287 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1. Issue 5 (1st May 2002) Authors: Hutter, P; Wijnen, J; Rey-Berthod, C; Thiffault, I; Verkuijlen, P; Farber, D; Hamel, N; Bapat, B; Thibodeau, S N; Burn, J; Wu, J; MacNamara, E; Heinimann, K; Chong, G; Foulkes, W D Journal: Journal of medical genetics Issue: Volume 39:Issue 5(2002) Page Start: 323 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. An unusual gait following the discovery of a new disease. Issue 2 (8th March 2011) Authors: Keogh, M J; Khan, A; Gorman, G; McNeill, A; Horvath, R; Burn, J; Chinnery, P F Journal: Practical neurology Issue: Volume 11:Issue 2(2011) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Angelman (happy puppet) syndrome in a girl and her brother. Issue 5 (May 1987) Authors: Fisher, J A; Burn, J; Alexander, F W; Gardner-Medwin, D Journal: Journal of medical genetics Issue: Volume 24:Issue 5(1987) Page Start: 294 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Association of less common cystic fibrosis mutations with a mild phenotype. Issue 1 (January 1991) Authors: Curtis, A; Nelson, R; Porteous, M; Burn, J; Bhattacharya, S S Journal: Journal of medical genetics Issue: Volume 28:Issue 1(1991) Page Start: 34 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Autosomal dominant thoracolaryngopelvic dysplasia: Barnes syndrome. Issue 4 (August 1986) Authors: Burn, J; Hall, C; Marsden, D; Matthew, D J Journal: Journal of medical genetics Issue: Volume 23:Issue 4(1986) Page Start: 345 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Behavioural phenotype of Cornelia de Lange syndrome. Issue 4 (1st October 1999) Authors: Berney, T P; Ireland, M; Burn, J Journal: Archives of disease in childhood Issue: Volume 81:Issue 4(1999) Page Start: 333 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Cell kinetics and gene expression changes in colorectal cancer patients given resistant starch: a randomised controlled trial. Issue 3 (31st October 2008) Authors: Dronamraju, S S; Coxhead, J M; Kelly, S B; Burn, J; Mathers, J C Journal: Gut Issue: Volume 58:Issue 3(2009) Page Start: 413 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗