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Publications by N. Chatron

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

English

MED13L-related Intellectual Disability: Involvement of Missense Variants and Delineation of the Phenotype

Molecular Neuroscience

English