Broadening of cohesinopathies: Exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype

Ilaria Parenti, Cristina Gervasini, Jelena Pozojevic, Luitgard Graul-Neumann, Jacopo Azzollini, Diana Braunholz, E. Watrin, K. S. Wendt, Anna Cereda, Davide Cittaro, Gabriele Gillessen-Kaesbach, Dejan Lazarevic, Milena Mariani, Silvia Russo, R. Werner, Peter Krawitz, Lidia Larizza, Angelo Selicorni, Frank J. Kaiser

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Medicine & Life Sciences