1. Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8). Issue 3 (March 1988) Authors: Quarrell, O W; Youngman, S; Sarfarazi, M; Harper, P S Journal: Journal of medical genetics Issue: Volume 25:Issue 3(1988) Page Start: 191 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphism. Issue 4 (April 1995) Authors: Pilz, D T; Dalton, A; Long, A; Jaspan, T; Maltby, E L; Quarrell, O W Journal: Journal of medical genetics Issue: Volume 32:Issue 4(1995) Page Start: 275 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Exclusion testing in pregnancy for Huntington's disease. Issue 8 (August 1990) Authors: Tyler, A; Quarrell, O W; Lazarou, L P; Meredith, A L; Harper, P S Journal: Journal of medical genetics Issue: Volume 27:Issue 8(1990) Page Start: 488 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome. Issue 5 (May 1995) Authors: Froggatt, N J; Koch, J; Davies, R; Evans, D G; Clamp, A; Quarrell, O W; Weissenbach, J; Hodgson, S V; Ponder, B A; Barton, D E Journal: Journal of medical genetics Issue: Volume 32:Issue 5(1995) Page Start: 352 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea. Issue 12 (December 1993) Authors: MacMillan, J C; Morrison, P J; Nevin, N C; Shaw, D J; Harper, P S; Quarrell, O W; Snell, R G Journal: Journal of medical genetics Issue: Volume 30:Issue 12(1993) Page Start: 1012 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities. Issue 1 (January 1990) Authors: Curtis, M A; Quarrell, O W; Cobon, A M; Cummins, M Journal: Journal of medical genetics Issue: Volume 27:Issue 1(1990) Page Start: 64 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Linkage disequilibrium in Huntington's disease: an improved localisation for the gene. Issue 11 (November 1989) Authors: Snell, R G; Lazarou, L P; Youngman, S; Quarrell, O W; Wasmuth, J J; Shaw, D J; Harper, P S Journal: Journal of medical genetics Issue: Volume 26:Issue 11(1989) Page Start: 673 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Liver histology in the arthrogryposis multiplex congenita, renal dysfunction, and cholestasis (ARC) syndrome: report of three new cases and review. Issue 1 (January 1994) Authors: Horslen, S P; Quarrell, O W; Tanner, M S Journal: Journal of medical genetics Issue: Volume 31:Issue 1(1994) Page Start: 62 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Maxillonasal dysplasia (Binder's syndrome). Issue 6 (June 1990) Authors: Quarrell, O W; Koch, M; Hughes, H E Journal: Journal of medical genetics Issue: Volume 27:Issue 6(1990) Page Start: 384 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD). Issue 4 (April 1994) Authors: Pilz, D; Quarrell, O W; Jones, E W Journal: Journal of medical genetics Issue: Volume 31:Issue 4(1994) Page Start: 328 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗