Affiliations 

  • 1 Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland
  • 2 Division of Human Genetics, 22q and You Center, and Clinical Genetics Center, The Children's Hospital of Philadelphia and the Department of Pediatrics at the Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania
  • 3 Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Health System, Washington, D.C
  • 4 Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China
  • 5 Faculty of Medicine, Department of Paediatrics, University of Malaya, Kuala Lumpur, Malaysia
  • 6 Faculty of Medicine, Human Genetics Unit, University of Colombo, Sri Lanka
  • 7 Center of Excellence for Medical Genetics, Faculty of Medicine, Department of Pediatrics, Chulalongkorn University, Bangkok, Thailand
  • 8 Department of Paediatrics College of Medicine, University of Lagos, Lagos University Teaching, Lagos, Nigeria
  • 9 Division of Genetics and Metabolism, Children's National Health System, Washington, D.C
  • 10 Mazumdar Shaw Medical Center, Narayana Health City, Bangalore, India
  • 11 Division of Medical Genetics, Department of Pediatrics, University of Mississippi Medical Center, Jackson, Mississippi
  • 12 Center of Human Genetics/School of Medicine and Pharmacy, College of Medicine and Health Sciences, University of Rwanda, Kigali, Rwanda
  • 13 Servicio de Genética, Hospital de Pediatría Garrahan, Buenos Aires, Argentina
  • 14 Hospital for the Rehabilitation of Craniofacial Anomalies, São Paulo University, Bauru, Brazil
  • 15 Department of Medical Genetics, University of Campinas, São Paulo, Brazil
  • 16 Center for Research on Genomics and Global Health, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland
Am J Med Genet A, 2017 Apr;173(4):i.
PMID: 28328119 DOI: 10.1002/ajmg.a.38224

Abstract

The cover image, by Paul Kruszka et al., is based on the Original Article 22q11.2 deletion syndrome in diverse populations, DOI: 10.1002/ajmg.a.38199. Individual images are property of the National Human Genome Research Institute and are in the public domain.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.