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

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Description scientific article published on 4 February 2015
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author: Davide Cittaro  Peter Krawitz  Dejan Lazarevic  Erwan Watrin  Jacopo Azzollini 

Publication date February 25, 2015
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