1. 21-hydroxylase deficiency families with HLA identical affected and unaffected sibs. Issue 1 (January 1989) Authors: Sinnott, P J; Dyer, P A; Price, D A; Harris, R; Strachan, T Journal: Journal of medical genetics Issue: Volume 26:Issue 1(1989) Page Start: 10 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21. Issue 9 (September 1994) Authors: Munro, C S; Carter, S; Bryce, S; Hall, M; Rees, J L; Kunkeler, L; Stephenson, A; Strachan, T Journal: Journal of medical genetics Issue: Volume 31:Issue 9(1994) Page Start: 675 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity. Issue 12 (December 1992) Authors: Evans, D G; Huson, S M; Donnai, D; Neary, W; Blair, V; Teare, D; Newton, V; Strachan, T; Ramsden, R; Harris, R Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 841 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counselling. Issue 12 (December 1992) Authors: Evans, D G; Huson, S M; Donnai, D; Neary, W; Blair, V; Newton, V; Strachan, T; Harris, R Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 847 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Antenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Issue 9 (September 1989) Authors: Strachan, T; Price, D A; Brook, C G D; Rumsby, G Journal: Archives of disease in childhood Issue: Volume 64:Issue 9(1989) Page Start: 1344 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Autosomal dominant sacral agenesis: Currarino syndrome. Issue 8 (1st August 2000) Authors: Lynch, Sally Ann; Wang, Yiming; Strachan, T; Burn, John; Lindsay, Susan Journal: Journal of medical genetics Issue: Volume 37:Issue 8(2000) Page Start: 561 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Diagnostic issues in a family with late onset type 2 neurofibromatosis. Issue 6 (June 1995) Authors: Evans, D G; Bourn, D; Wallace, A; Ramsden, R T; Mitchell, J D; Strachan, T Journal: Journal of medical genetics Issue: Volume 32:Issue 6(1995) Page Start: 470 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genetics and genomics in medicine. (2022) Authors: Strachan, T; Lucassen, Anneke Record Type: Book Extent: 1 online resource, illustrations (colour) View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations. Issue 6 (June 1998) Authors: Evans, D G; Trueman, L; Wallace, A; Collins, S; Strachan, T Journal: Journal of medical genetics Issue: Volume 35:Issue 6(1998) Page Start: 450 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Human Immunogenetics. Basic Principles and Clinical Relevance. Issue 5 (May 1990) Authors: Strachan, T Journal: Journal of medical genetics Issue: Volume 27:Issue 5(1990) Page Start: 342 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗