The spectrum of heart defects in the TRAF7-related multiple congenital anomalies-intellectual disability syndrome

Affiliations

• ¹ Laboratory of embryology and genetics of human malformations, INSERM Unité Mixte de Recherche 1163, Institut Imagine and Université Paris Cité, Paris 75015, France.
• ² Human Genetics, Department of Life, Health and Environmental Sciences, University of L'Aquila, Coppito 67100, L'Aquila, Italy.
• ³ Human Functional Genomics Laboratory, Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele Roma, Rome 00163, Italy.
• ⁴ Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322.
• ⁵ Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104.
• ⁶ Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104.
• ⁷ Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.
• ⁸ Department of Pediatrics, School of Medicine, University of Washington, Seattle, WA 98105.
• ⁹ Alberta Children's Hospital, University of Calgary, Calgary, AB T2N 4N1, Canada.
• ¹⁰ Service de Génétique Médicale, Centre Hospitalo-Universitaire de Bordeaux, Bordeaux F-33000, France.
• ¹¹ Centre de Génétique Humaine, Centre Hospitalo-Universitaire de Besançon, Besançon 25000, France.
• ¹² Department of Medical Genetics, Haukeland University Hospital, Bergen 5021, Norway.
• ¹³ Department of Medical Genetics, St. Olavs Hospital, Trondheim University Hospital, Trondheim 7006, Norway.
• ¹⁴ Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund 4293, Denmark.
• ¹⁵ Department of Genetics, Rigshospitalet, Copenhagen 2100, Denmark.
• ¹⁶ Department of Human Genetics, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA 90095.
• ¹⁷ Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.
• ¹⁸ Department of Clinical Genetics, St. Michaels Hospital, University Hospitals Bristol and Weston National Health Service Trust, Bristol BS2 8EJ, United Kingdom.
• ¹⁹ Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ 85012.
• ²⁰ Medical Genetics Laboratory, Azienda Sociosanitaria Territoriale Papa Giovanni XXIII, Bergamo 24127, Italy.
• ²¹ Unit of Medical Genetics, Azienda Ospedaliera di Rilievo Nazionale Cardarelli, Naples 80131, Italy.
• ²² Department of Medical Sciences, University of Torino, Torino 10124, Italy.
• ²³ Immunogenetics and Transplant Biology Unit, Città della Salute e della Scienza University Hospital, Torino 10126, Italy.
• ²⁴ Pediatric Clinical Genetics Unit, Ospedale Infantile Regina Margherita, Department of Public Health and Pediatric Sciences, University of Torino, Torino 10126, Italy.
• ²⁵ Department of Clinical Genetics, Leiden University Medical Centre, 2300 RC Leiden, the Netherlands.
• ²⁶ Department of Pathology, Medical College of Wisconsin, Milwaukee, WI 53223.
• ²⁷ Biostatistics Unit, Université Paris Cité, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris 75015, France.
• ²⁸ Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris 75015, France.