The spectrum of heart defects in the TRAF7 -related multiple congenital anomalies-intellectual disability syndrome.
- Resource Type
- Editorial & Opinion
- Authors
- Pisan E; Laboratory of embryology and genetics of human malformations, INSERM Unité Mixte de Recherche 1163, Institut Imagine and Université Paris Cité, Paris 75015, France.; De Luca C; Human Genetics, Department of Life, Health and Environmental Sciences, University of L'Aquila, Coppito 67100, L'Aquila, Italy.; Brancati F; Human Genetics, Department of Life, Health and Environmental Sciences, University of L'Aquila, Coppito 67100, L'Aquila, Italy.; Human Functional Genomics Laboratory, Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele Roma, Rome 00163, Italy.; Sanchez Russo R; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322.; Li D; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104.; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.; Bhoj E; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104.; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.; Wenger T; Department of Pediatrics, School of Medicine, University of Washington, Seattle, WA 98105.; Marwaha A; Alberta Children's Hospital, University of Calgary, Calgary, AB T2N 4N1, Canada.; Johnson N; Alberta Children's Hospital, University of Calgary, Calgary, AB T2N 4N1, Canada.; Beneteau C; Service de Génétique Médicale, Centre Hospitalo-Universitaire de Bordeaux, Bordeaux F-33000, France.; Brischoux-Boucher E; Centre de Génétique Humaine, Centre Hospitalo-Universitaire de Besançon, Besançon 25000, France.; Houge G; Department of Medical Genetics, Haukeland University Hospital, Bergen 5021, Norway.; Paulsen J; Department of Medical Genetics, St. Olavs Hospital, Trondheim University Hospital, Trondheim 7006, Norway.; Hammer TB; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund 4293, Denmark.; Department of Genetics, Rigshospitalet, Copenhagen 2100, Denmark.; Ek J; Department of Genetics, Rigshospitalet, Copenhagen 2100, Denmark.; Schweitzer D; Department of Human Genetics, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA 90095.; Russell BE; Department of Human Genetics, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA 90095.; Dutra-Clarke M; Department of Human Genetics, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA 90095.; Nelson S; Department of Human Genetics, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA 90095.; Douine ED; Department of Human Genetics, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA 90095.; Corona RI; Department of Human Genetics, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA 90095.; Dudding T; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.; Thomson H; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.; Low K; Department of Clinical Genetics, St. Michaels Hospital, University Hospitals Bristol and Weston National Health Service Trust, Bristol BS2 8EJ, United Kingdom.; Belnap N; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ 85012.; Iascone M; Medical Genetics Laboratory, Azienda Sociosanitaria Territoriale Papa Giovanni XXIII, Bergamo 24127, Italy.; Priolo M; Unit of Medical Genetics, Azienda Ospedaliera di Rilievo Nazionale Cardarelli, Naples 80131, Italy.; Carli D; Department of Medical Sciences, University of Torino, Torino 10124, Italy.; Immunogenetics and Transplant Biology Unit, Città della Salute e della Scienza University Hospital, Torino 10126, Italy.; Mussa A; Pediatric Clinical Genetics Unit, Ospedale Infantile Regina Margherita, Department of Public Health and Pediatric Sciences, University of Torino, Torino 10126, Italy.; Bijlsma EK; Department of Clinical Genetics, Leiden University Medical Centre, 2300 RC Leiden, the Netherlands.; Kopp N; Department of Pathology, Medical College of Wisconsin, Milwaukee, WI 53223.; Jais JP; Biostatistics Unit, Université Paris Cité, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris 75015, France.; Amiel J; Laboratory of embryology and genetics of human malformations, INSERM Unité Mixte de Recherche 1163, Institut Imagine and Université Paris Cité, Paris 75015, France.; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris 75015, France.; Gordon CT; Laboratory of embryology and genetics of human malformations, INSERM Unité Mixte de Recherche 1163, Institut Imagine and Université Paris Cité, Paris 75015, France.
- Source
- Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1091-6490 (Electronic) Linking ISSN: 00278424 NLM ISO Abbreviation: Proc Natl Acad Sci U S A Subsets: MEDLINE
- Subject
- Language
- English
Competing Interests: Competing interests statement:The authors declare no competing interest.