1. 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) ↗
2. 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) ↗