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Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.Neurogenetics|March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotypeT Smol, F Petit, A Piton, et al.Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.Pageof 67