1. 7q11.23 Microduplication: a recognizable phenotype. (8th April 2012) Authors: Dixit, A; McKee, S; Mansour, S; Mehta, SG; Tanteles, GA; Anastasiadou, V; Patsalis, PC; Martin, K; McCullough, S; Suri, M; Sarkar, A Journal: Clinical genetics Issue: Volume 83:Number 2(2013:Feb.) Page Start: 155 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A clinical and genetic study of campomelic dysplasia. Issue 6 (June 1995) Authors: Mansour, S; Hall, C M; Pembrey, M E; Young, I D Journal: Journal of medical genetics Issue: Volume 32:Issue 6(1995) Page Start: 415 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A diagnostic dilemma: aetiological diagnosis of lymphoedema patients at an Indian multidisciplinary meeting. Issue 1 (2019) Authors: Zanten, M van; Riches, K; Keeley, V; Mortimer, P; Ryan, T; Mansour, S; Narahari, S Journal: Journal of lymphoedema Issue: Volume 14:Issue 1(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family. (26th April 2013) Authors: Brice, G; Ostergaard, P; Jeffery, S; Gordon, K; Mortimer, PS; Mansour, S Journal: Clinical genetics Issue: Volume 84:Number 4(2013:Oct.) Page Start: 378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review. (1st February 2021) Authors: Dempsey, E; Haworth, A; Ive, L; Dubis, R; Savage, H; Serra, E; Kenny, J; Elmslie, F; Greco, E; Thilaganathan, B; Mansour, S; Homfray, T; Drury, S Journal: BJOG Issue: Volume 128:Number 6(2021) Page Start: 1012 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Accelerated atherosclerosis following intracoronary haematopoietic stem cell administration. Issue 4 (16th March 2005) Authors: Vanderheyden, M; Mansour, S; Bartunek, J Journal: Heart Issue: Volume 91:Issue 4(2005) Page Start: 448 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. Issue 7 (1st July 2002) Authors: Brice, G; Mansour, S; Bell, R; Collin, J R O; Child, A H; Brady, A F; Sarfarazi, M; Burnand, K G; Jeffery, S; Mortimer, P; Murday, V A Journal: Journal of medical genetics Issue: Volume 39:Issue 7(2002) Page Start: 478 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Appendicitis risk prediction models in children presenting with right iliac fossa pain (RIFT study): a prospective, multicentre validation study. (April 2020) Authors: Nepogodiev, Dmitri; Wilkin, Richard JW; Bradshaw, Catherine J; Skerritt, Clare; Ball, Alasdair; Moni-Nwinia, Waaka; Blanco-Colino, Ruth; Chauhan, Priyesh; Drake, Thomas M; Frasson, Matteo; Gee, Oliver; Glasbey, James C; Matthews, Jacob H; Morley, Gabriella L; Naumann, David N; Pata, Francesco; So... Journal: Lancet Issue: Volume 4:Number 4(2020) Page Start: 271 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Celastrol protects ischaemic myocardium through a heat shock response with up‐regulation of haeme oxygenase‐1. (December 2014) Authors: Der Sarkissian, S; Cailhier, J‐F; Borie, M; Stevens, L‐M; Gaboury, L; Mansour, S; Hamet, P; Noiseux, N Journal: British journal of pharmacology Issue: Volume 171:Number 23(2014:Dec.) Page Start: 5265 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes. Issue 12 (18th December 2003) Authors: Oosterwijk, J C; Mansour, S; van Noort, G; Waterham, H R; Hall, C M; Hennekam, R C M Journal: Journal of medical genetics Issue: Volume 40:Issue 12(2003) Page Start: 937 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗