Cite
MLA Citation
María Concepción Gil‐Rodríguez et al.. “De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome‐Overlapping Phenotypes.” Human mutation, vol. 36, no. 4, n.d., pp. 454–462. http://access.bl.uk/ark:/81055/vdc_100025022748.0x00005a