Exome analysis of Smith–Magenis-like syndrome cohort identifies de novo likely pathogenic variants

Seth I. Berger,C. Ciccone,Karen L. Simon,M. Malicdan,T. Vilboux,C. Billington,Roxanne E. Fischer,W. Introne,A. Gropman,J. Blancato,J. Mullikin,W. Gahl,M. Huizing,Ann C M Smith,Nisc Comparative Sequencing Program

Published 2017 in Human Genetics

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