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Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomalies von Alby, Caroline, Boutaud, Lucile, Bessières, Bettina, Serre, Valérie, Rio, Marlene, Cormier‐Daire, Valerie, de Oliveira, Judith, Ichkou, Amale, Mouthon, Linda, Gordon, Christopher T., Bonnière, Maryse, Mechler, Charlotte, Nitschke, Patrick, Bole, Christine, Lyonnet, Stanislas, Bahi‐Buisson, Nadia, Boddaert, Nathalie, Colleaux, Laurence, Roth, Philippe, Ville, Yves, Vekemans, Michel, Encha‐Razavi, Féréchté, Attié‐Bitach, Tania, Thomas, Sophie

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