1. A complex chromosomal rearrangement with formation of a ring 4. Issue 2 (June 1971) Authors: Bobrow, M; Joness, L F; Clarke, G Journal: Journal of medical genetics Issue: Volume 8:Issue 2(1971) Page Start: 235 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods. Issue 5 (May 1991) Authors: Abbs, S; Yau, S C; Clark, S; Mathew, C G; Bobrow, M Journal: Journal of medical genetics Issue: Volume 28:Issue 5(1991) Page Start: 304 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A giant short arm of no. 21 chromosome in mother of 21/21 translocation mongol. Issue 5 (October 1976) Authors: Tuncbilek, E; Bobrow, M; Clarke, G; Taysi, K Journal: Journal of medical genetics Issue: Volume 13:Issue 5(1976) Page Start: 411 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE loci. Issue 3 (March 1995) Authors: Wang, Q; Green, E; Bobrow, M; Mathew, C G Journal: Journal of medical genetics Issue: Volume 32:Issue 3(1995) Page Start: 170 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis. Issue 7 (July 1996) Authors: Yau, S C; Bobrow, M; Mathew, C G; Abbs, S J Journal: Journal of medical genetics Issue: Volume 33:Issue 7(1996) Page Start: 550 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Analysis of national register of Down's syndrome in England and Wales: trends in prenatal diagnosis, 1989-91. Issue 6875 (13th February 1993) Authors: Mutton, D E; Ide, R; Alberman, E; Bobrow, M Journal: BMJ Issue: Volume 306:Issue 6875(1993) Page Start: 431 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene. Issue 3 (March 1992) Authors: Abbs, S; Bobrow, M Journal: Journal of medical genetics Issue: Volume 29:Issue 3(1992) Page Start: 191 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11–17 distinct from the GAP related domain. Issue 4 (1st April 2004) Authors: Mattocks, C; Baralle, D; Tarpey, P; ffrench-Constant, C; Bobrow, M; Whittaker, J Journal: Journal of medical genetics Issue: Volume 41:Issue 4(2004) Page Start: e48 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British Isles. Issue 8 (August 1992) Authors: Landels, E C; Green, P M; Ellis, I H; Fensom, A H; Bobrow, M Journal: Journal of medical genetics Issue: Volume 29:Issue 8(1992) Page Start: 563 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Better quality data for Down's syndrome register. Issue 6891 (5th June 1993) Authors: Mutton, D; Alberman, E; Ide, R; Bobrow, M Journal: BMJ Issue: Volume 306:Issue 6891(1993) Page Start: 1541 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗