The same genomic variants in the first three exons of KANSL1 can be either benign or causative of Koolen-de Vries syndrome: Definition of a validation procedure by Federica Francesca L'Erario, Giuseppe Marangi, Anna Gloria Renzi, Marina Carapelle, Paolo Niccolò Doronzio, Domizia Pasquetti, Sabrina Maietta, Elena Sonnini, Annalisa Gazzellone, Marcella Zollino

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