1. Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6. Issue 5 (18th April 2006) Authors: O'Connor, E; Allen, L E; Bradshaw, K; Boylan, J; Moore, A T; Trump, D Journal: British journal of ophthalmology Issue: Volume 90:Issue 5(2006) Page Start: 653 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Connexin variations and deafness. (29th September 2015) Authors: Rangan, S; Umapathy, D; Kennedy, V; Belk, R; Trump, D Journal: Archives of disease in childhood Issue: Volume 95:Supplement 1(2010) Page Start: A109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genotype-phenotype correlation in British families with X linked congenital stationary night blindness. Issue 11 (10th November 2003) Authors: Allen, L E; Zito, I; Bradshaw, K; Patel, R J; Bird, A C; Fitzke, F; Yates, J R; Trump, D; Hardcastle, A J; Moore, A T Journal: British journal of ophthalmology Issue: Volume 87:Issue 11(2003) Page Start: 1413 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27. Issue 11 (November 1998) Authors: Trump, D; Dixon, P H; Mumm, S; Wooding, C; Davies, K E; Schlessinger, D; Whyte, M P; Thakker, R V Journal: Journal of medical genetics Issue: Volume 35:Issue 11(1998) Page Start: 905 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis. Issue 6 (19th February 2008) Authors: Hadfield, K D; Newman, W G; Bowers, N L; Wallace, A; Bolger, C; Colley, A; McCann, E; Trump, D; Prescott, T; Evans, D G R Journal: Journal of medical genetics Issue: Volume 45:Issue 6(2008) Page Start: 332 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Molecular pathology of X linked retinoschisis: mutations interfere with retinoschisin secretion and oligomerisation. Issue 1 (16th December 2005) Authors: Wang, T; Zhou, A; Waters, C T; O'Connor, E; Read, R J; Trump, D Journal: British journal of ophthalmology Issue: Volume 90:Issue 1(2006) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Myoclonic movement disorder associated with microdeletion of chromosome 22q11. Issue 5 (1st November 2002) Authors: Baralle, D; Trump, D; ffrench-Constant, C; Dick, D J Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 73:Issue 5(2002) Page Start: 600 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Neurofibromatosis 2 in a patient with a de novo balanced reciprocal translocation 46, X, t(X;22)(p11.2;q11.2). Issue 9 (5th September 2003) Authors: Bovie, C; Holden, S T; Schroer, A; Smith, E; Trump, D; Raymond, F L Journal: Journal of medical genetics Issue: Volume 40:Issue 9(2003) Page Start: 682 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. SMARCB1 mutations are not a common cause of multiple meningiomas. Issue 8 (14th May 2010) Authors: Hadfield, K D; Smith, M J; Trump, D; Newman, W G; Evans, D G Journal: Journal of medical genetics Issue: Volume 47:Issue 8(2010) Page Start: 567 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Temperature sensitive oculocutaneous albinism associated with missense changes in the tyrosinase gene. Issue 10 (16th September 2005) Authors: Wang, T; Waters, C T; Jakins, T; Yates, J R W; Trump, D; Bradshaw, K; Moore, A T Journal: British journal of ophthalmology Issue: Volume 89:Issue 10(2005) Page Start: 1383 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗