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HARVARD Citation
Parenti, I. et al. (2016). Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange‐overlapping phenotype. Clinical genetics. 89 (1), pp. 74-81. [Online].
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Parenti, I. et al. (2016). Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange‐overlapping phenotype. Clinical genetics. 89 (1), pp. 74-81. [Online].