1. A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. Issue 12 (26th October 2010) Authors: Darvish, H; Esmaeeli-Nieh, S; Monajemi, G B; Mohseni, M; Ghasemi-Firouzabadi, S; Abedini, S S; Bahman, I; Jamali, P; Azimi, S; Mojahedi, F; Dehghan, A; Shafeghati, Y; Jankhah, A; Falah, M; Soltani Banavandi, M J; Ghani-Kakhi, M; Garshasbi, M; Rakhshani, F; Naghavi, A; Tzschach, A Journal: Journal of medical genetics Issue: Volume 47:Issue 12(2010) Page Start: 823 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 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) ↗
3. Novel SLC9A6 mutations in two families with Christianson syndrome. (30th August 2012) Authors: Riess, A; Rossier, E; Krüger, R; Dufke, A; Beck‐Woedl, S; Horber, V; Alber, M; Gläser, D; Riess, O; Tzschach, A Journal: Clinical genetics Issue: Volume 83:Number 6(2013:Jun.) Page Start: 596 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). (19th April 2013) Authors: Hoffer, JL; Fryssira, H; Konstantinidou, AE; Ropers, H−H; Tzschach, A Journal: Clinical genetics Issue: Volume 83:Number 1(2013:Jan.) Page Start: 92 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). (9th April 2012) Authors: Hoffer, JL; Fryssira, H; Konstantinidou, AE; Ropers, H−H; Tzschach, A Journal: Clinical genetics Issue: Volume 83:Number 1(2013:Jan.) Page Start: 92 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗