1. Osteogenesis imperfecta, tricho‐dento‐osseous syndrome and intellectual disability: A familial case with 17q21.33‐q22 (COL1A1 and DLX3) deletion and 7q32.3‐q33 duplication resulting from a reciprocal interchromosomal insertion. Issue 10 (15th August 2013) Authors: Harbuz, Radu; Bilan, Frédéric; Couet, Dominique; Charraud, Valérie; Kitzis, Alain; Gilbert‐Dussardier, Brigitte Journal: American journal of medical genetics Issue: Volume 161:Issue 10(2013:Oct.) Page Start: 2504 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗