Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype
Nature Genetics2012Vol. 44(6), pp. 636–638
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Marcella Zollino, Daniela Orteschi, Marina Murdolo, Serena Lattante, Domenica Battaglia, Chiara Stefanini, Eugenio Mercuri, Pietro Chiurazzi, Giovanni Neri, Giuseppe Marangi
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