1. A cytogenetic survey in Menkes disease: implications for the detection of chromosomal rearrangements in X linked disorders. Issue 4 (April 1993) Authors: Tommerup, N; Tümer, Z; Tønnesen, T; Horn, N Journal: Journal of medical genetics Issue: Volume 30:Issue 4(1993) Page Start: 314 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Breakpoints around the HOXD cluster result in various limb malformations. Issue 2 (24th June 2005) Authors: Dlugaszewska, B; Silahtaroglu, A; Menzel, C; Kübart, S; Cohen, M; Mundlos, S; Tümer, Z; Kjaer, K; Friedrich, U; Ropers, H-H; Tommerup, N; Neitzel, H; Kalscheuer, V M Journal: Journal of medical genetics Issue: Volume 43:Issue 2(2006) Page Start: 111 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. First trimester prenatal diagnosis of Menkes disease by DNA analysis. Issue 8 (August 1994) Authors: Tümer, Z; Tønnesen, T; Böhmann, J; Marg, W; Horn, N Journal: Journal of medical genetics Issue: Volume 31:Issue 8(1994) Page Start: 615 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic anticipation in Behçet's syndrome. Issue 1 (1st January 1998) Authors: Fresko, I; Soy, M; Hamuryudan, V; Yurdakul, S; Yavuz, Ş; Tümer, Z; Yazici, H Journal: Annals of the rheumatic diseases Issue: Volume 57:Issue 1(1998) Page Start: 45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease. Issue 11 (19th August 2008) Authors: Erdogan, F; Larsen, L A; Zhang, L; Tümer, Z; Tommerup, N; Chen, W; Jacobsen, J R; Schubert, M; Jurkatis, J; Tzschach, A; Ropers, H-H; Ullmann, R Journal: Journal of medical genetics Issue: Volume 45:Issue 11(2008) Page Start: 704 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mapping of 5q35 chromosomal rearrangements within a genomically unstable region. Issue 10 (15th July 2008) Authors: Buysse, K; Crepel, A; Menten, B; Pattyn, F; Antonacci, F; Veltman, J A; Larsen, L A; Tümer, Z; de Klein, A; van de Laar, I; Devriendt, K; Mortier, G; Speleman, F Journal: Journal of medical genetics Issue: Volume 45:Issue 10(2008) Page Start: 672 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Menkes disease: recent advances and new aspects. Issue 4 (April 1997) Authors: Tümer, Z; Horn, N Journal: Journal of medical genetics Issue: Volume 34:Issue 4(1997) Page Start: 265 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Not para-, not peri-, but centric inversion of chromosome 12. Issue 8 (August 1998) Authors: Silahtaroglu, A N; Hacihanefioglu, S; Güven, G S; Cenani, A; Wirth, J; Tommerup, N; Tümer, Z Journal: Journal of medical genetics Issue: Volume 35:Issue 8(1998) Page Start: 682 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutations. (22nd January 2013) Authors: Rendtorff, ND; Schrijver, I; Lodahl, M; Rodriguez‐Paris, J; Johnsen, T; Hansén, EC; Nickelsen, LAA; Tümer, Z; Fagerheim, T; Wetke, R; Tranebjærg, L Journal: Clinical genetics Issue: Volume 84:Number 4(2013:Oct.) Page Start: 388 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗