1. A novel pericentric inversion of chromosome 3 cosegregates with a developmental-behavioural phenotype. Issue 2 (1st February 2003) Authors: Efron, D; Delatycki, M B; de Silva, M G; Langbein, A; Slaghuis, W; Larson, A; Dahl, H-H M; Forrest, S M Journal: Journal of medical genetics Issue: Volume 40:Issue 2(2003) Page Start: e15 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3. Issue 9 (1st September 2004) Authors: Solomon, N M; Ross, S A; Morgan, T; Belsky, J L; Hol, F A; Karnes, P S; Hopwood, N J; Myers, S E; Tan, A S; Warne, G L; Forrest, S M; Thomas, P Q Journal: Journal of medical genetics Issue: Volume 41:Issue 9(2004) Page Start: 669 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Comparison of genotype and intellectual phenotype in untreated PKU patients. Issue 5 (May 1993) Authors: Ramus, S J; Forrest, S M; Pitt, D B; Saleeba, J A; Cotton, R G Journal: Journal of medical genetics Issue: Volume 30:Issue 5(1993) Page Start: 401 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Familial adenomatous polyposis in a 5 year old child: a clinical, pathological, and molecular genetic study. Issue 2 (February 1996) Authors: Distante, S; Nasioulas, S; Somers, G R; Cameron, D J; Young, M A; Forrest, S M; Gardner, R J Journal: Journal of medical genetics Issue: Volume 33:Issue 2(1996) Page Start: 157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Maternal uniparental disomy of chromosome 13 in a phenotypically normal child. Issue 8 (August 1994) Authors: Slater, H; Shaw, J H; Dawson, G; Bankier, A; Forrest, S M Journal: Journal of medical genetics Issue: Volume 31:Issue 8(1994) Page Start: 644 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctata. Issue 12 (December 1998) Authors: Sheffield, L J; Osborn, A H; Hutchison, W M; Sillence, D O; Forrest, S M; White, S J; Dahl, H H Journal: Journal of medical genetics Issue: Volume 35:Issue 12(1998) Page Start: 1004 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA gene. Issue 9 (September 1998) Authors: Delatycki, M B; Paris, D; Gardner, R J; Forshaw, K; Nicholson, G A; Nassif, N; Williamson, R; Forrest, S M Journal: Journal of medical genetics Issue: Volume 35:Issue 9(1998) Page Start: 713 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. UPD 13: no indication of maternal or paternal imprinting of genes on chromosome 13. Issue 6 (June 1995) Authors: Slater, H; Shaw, J H; Bankier, A; Forrest, S M; Dawson, G Journal: Journal of medical genetics Issue: Volume 32:Issue 6(1995) Page Start: 493 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗