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Jourdy, Y., Chatron, N., Carage, M., Fretigny, M., Meunier, S., Zawadzki, C., Gay, V., Negrier, C., Sanlaville, D., & Vinciguerra, C. (n.d.). study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability. Journal of thrombosis and haemostasis, 14, 1988–1993. http://access.bl.uk/ark:/81055/vdc_100038942953.0x000013