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Original article
Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation

Authors

  • Gregory Ryan Handrigan Undergraduate Medical Education, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • David Chitayat Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, CanadaPrenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Anath C Lionel Program in Genetics and Genome Biology, The Centre for Applied Genomics, Hospital for Sick Children, Toronto, OntarioDepartment of Molecular Genetics and McLaughlin Centre, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Maury Pinsk Department of Pediatrics, Pediatric Nephrology, University of Alberta, Edmonton, Alberta, Canada PubMed articlesGoogle scholar articles
  • Andrea K Vaags Program in Genetics and Genome Biology, The Centre for Applied Genomics, Hospital for Sick Children, Toronto, Ontario PubMed articlesGoogle scholar articles
  • Christian R Marshall Program in Genetics and Genome Biology, The Centre for Applied Genomics, Hospital for Sick Children, Toronto, OntarioDepartment of Molecular Genetics and McLaughlin Centre, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Sarah Dyack Department of Paediatrics, Dalhousie University, Halifax, Nova Scotia, Canada PubMed articlesGoogle scholar articles
  • Luis F Escobar Medical Genetics and Neurodevelopmental Center, Peyton Manning Children's Hospital, Indianapolis, Indiana, USA PubMed articlesGoogle scholar articles
  • Bridget A Fernandez Disciplines of Genetics and Medicine, Memorial University of Newfoundland, St. John's, Newfoundland and Labrador, Canada PubMed articlesGoogle scholar articles
  • Joseph C Stegman Developmental and Behavioral Clinic of the Carolinas, Concord, North Carolina, USA PubMed articlesGoogle scholar articles
  • Jill A Rosenfeld Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington, USA PubMed articlesGoogle scholar articles
  • Lisa G Shaffer Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington, USA PubMed articlesGoogle scholar articles
  • McKinsey Goodenberger Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA PubMed articlesGoogle scholar articles
  • Jennelle C Hodge Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA PubMed articlesGoogle scholar articles
  • Jason E Cain Division of Nephrology and Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Riyana Babul-Hirji Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Dimitri J Stavropoulos Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, CanadaDepartment of Pediatric Laboratory Medicine, Cytogenetics Laboratory, Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Verna Yiu Department of Pediatrics, Pediatric Nephrology, University of Alberta, Edmonton, Alberta, Canada PubMed articlesGoogle scholar articles
  • Stephen W Scherer Program in Genetics and Genome Biology, The Centre for Applied Genomics, Hospital for Sick Children, Toronto, OntarioDepartment of Molecular Genetics and McLaughlin Centre, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Norman D Rosenblum Division of Nephrology and Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, CanadaDepartment of Physiology, University of Toronto, Toronto, Ontario, CanadaDepartment of Paediatrics, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Norman D. Rosenblum, Division of Nephrology, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, Canada M5G1X8; norman.rosenblum{at}sickkids.ca
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Citation

Handrigan GR, Chitayat D, Lionel AC, et al
Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation

Publication history

  • Received September 7, 2012
  • Revised November 17, 2012
  • Accepted December 7, 2012
  • First published January 18, 2013.
Online issue publication 
February 13, 2013

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