1. Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations. Issue 4 (26th October 2007) Authors: Witsch-Baumgartner, M; Schwentner, I; Gruber, M; Benlian, P; Bertranpetit, J; Bieth, E; Chevy, F; Clusellas, N; Estivill, X; Gasparini, G; Giros, M; Kelley, R I; Krajewska-Walasek, M; Menzel, J; Miettinen, T; Ogorelkova, M; Rossi, M; Scala, I; Schinzel, A; Schmidt, K Journal: Journal of medical genetics Issue: Volume 45:Issue 4(2008) Page Start: 200 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay. Issue 9 (1st September 2001) Authors: Syrrou, M; Fryns, J-P Journal: Journal of medical genetics Issue: Volume 38:Issue 9(2001) Page Start: 621 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Mosaicism for duplication 12q (12q13→12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant. Issue 11 (1st November 2002) Authors: Vermeesch, J R; Syrrou, M; Salden, I; Dhondt, F; Matthijs, G; Fryns, J-P Journal: Journal of medical genetics Issue: Volume 39:Issue 11(2002) Page Start: e72 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗