Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability
Yohann Jourdy(Hospices Civils de Lyon), Christine Vinciguerra(Université Claude Bernard Lyon 1), Valérie Gay(Centre Hospitalier Métropole Savoie), Sandrine Meunier(Lille’s Cardiology Hospital), Mathilde Frétigny(Hospices Civils de Lyon), Damien Sanlaville(Hospices Civils de Lyon), Nicolas Chatron(Hospices Civils de Lyon), M.‐L. Carage(Hospices Civils de Lyon), C. Zawadzki(Centre Hospitalier Universitaire de Lille), Claude Négrier(Université Claude Bernard Lyon 1)
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