Exome analysis of Smith–Magenis-like syndrome cohort identifies de novo likely pathogenic variants
Ann C. M. Smith(Children's Hospital Colorado), Thierry Vilboux(Inova Health System), Wendy J. Introne, May Christine V. Malicdan(National Institutes of Health), Andrea Gropman(Children's National), James C. Mullikin(Human Genome Sciences (United States)), Jan Blancato(Georgetown University), Seth Berger(Children's National), William A. Gahl(National Institute of Child Health), Karen L. Simon(National Institutes of Health), Marjan Huizing(National Human Genome Research Institute), Charles J. Billington(University of Minnesota System), Roxanne Fischer(National Institutes of Health), Carla Ciccone(National Institutes of Health)
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