1. Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?. Issue 4 (April 1994) Authors: Fewtrell, M S; Tam, P K; Thomson, A H; Fitchett, M; Currie, J; Huson, S M; Mulligan, L M Journal: Journal of medical genetics Issue: Volume 31:Issue 4(1994) Page Start: 325 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus. Issue 8 (August 1994) Authors: Edery, P; Pelet, A; Mulligan, L M; Abel, L; Attié, T; Dow, E; Bonneau, D; David, A; Flintoff, W; Jan, D Journal: Journal of medical genetics Issue: Volume 31:Issue 8(1994) Page Start: 602 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas. Issue 12 (December 1995) Authors: Eng, C; Crossey, P A; Mulligan, L M; Healey, C S; Houghton, C; Prowse, A; Chew, S L; Dahia, P L; O'Riordan, J L; Toledo, S P Journal: Journal of medical genetics Issue: Volume 32:Issue 12(1995) Page Start: 934 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Reconsideration of biallelic inactivation of theVHL tumour suppressor gene in hemangioblastomas of the central nervous system. Issue 5 (1st May 2001) Authors: Gläsker, S; Bender, B U; Apel, T W; van Velthoven, V; Mulligan, L M; Zentner, J; Neumann, H P H Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 70:Issue 5(2001) Page Start: 644 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗