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

I. Parenti, C. Gervasini, J. Pozojevic, L. Graul-Neumann, J. Azzollini, D. Braunholz, E. Watrin, K. S. Wendt, A. Cereda, D. Cittaro, G. Gillessen-Kaesbach, D. Lazarevic, M. Mariani, S. Russo, R. Werner, P. Krawitz, L. Larizza, A. Selicorni, F. J. Kaiser*

*Corresponding author for this work
25 Citations (Scopus)

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