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
Titel:
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
Auteur:
L'Erario, Federica Francesca Marangi, Giuseppe Renzi, Anna Gloria Carapelle, Marina Doronzio, Paolo Niccolò Pasquetti, Domizia Maietta, Sabrina Sonnini, Elena Gazzellone, Annalisa Zollino, Marcella