De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome‐Overlapping Phenotypes

Publisher： John Wiley & Sons Inc

E-ISSN： 1098-1004|36|4|454-462

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.36, Iss.4, 2015-04, pp. : 454-462

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