1. Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability. (17th September 2016) Authors: Jourdy, Y.; Chatron, N.; Carage, M.‐L.; Fretigny, M.; Meunier, S.; Zawadzki, C.; Gay, V.; Negrier, C.; Sanlaville, D.; Vinciguerra, C. Journal: Journal of thrombosis and haemostasis Issue: Volume 14:Number 10(2016:Oct.) Page Start: 1988 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗