A boy with dysmorphic features, intellectual disability, and biallelic homozygous deletion in NRXN1

Department of Paediatrics, Skåne University Hospital, Lund, Sweden Correspondence to Peter Holmquist, MD, Department of Paediatrics, Skåne University Hospital, Lund 22185, Sweden Tel: +46 46 17 10 00; e-mail: [email protected] Received May 2, 2014 Accepted November 11, 2014