Cite
HARVARD Citation
Gil‐Rodríguez, M. et al. (n.d.). De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome‐Overlapping Phenotypes. Human mutation. 36 (4), pp. 454-462. [Online].
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Gil‐Rodríguez, M. et al. (n.d.). De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome‐Overlapping Phenotypes. Human mutation. 36 (4), pp. 454-462. [Online].