The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant

Overview of attention for article published in European Journal of Human Genetics, August 2015

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Want to learn more about the phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant? Read on here! https://t.co/pwgeiAGclL #KdVSFoundation #KdVS #KoolendeVriesSyndrome

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