De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas.

Journal: American Journal of Human Genetics

Published: 2020-06-04

DOI: 10.1016/j.ajhg.2020.04.015

Affiliations: 36

Authors: 57

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Institutions Share
Division of Orthopaedic Surgery, CHOP, United States of America (USA) 0.11
GeneDx Inc., United States of America (USA) 0.07
Institute of Human Genetics, UDE, Germany 0.06
Division of Human Genetics, CHOP, United States of America (USA) 0.05
University Hospital Nantes (CHU de Nantes), France 0.05
Clinical Institute of Medical Genetics, UMCL, Slovenia 0.04
Roberts Individualized Medical Genetics Center (IMGC), CHOP, United States of America (USA) 0.04
Duke Department of Pediatrics, United States of America (USA) 0.04
Center for Human Genetics (CME), Belgium 0.04
Cibles Moléculaires et Thérapeutique de la Maladie d'Alzheimer, France 0.04
Department of Clinical Genetics, Leiden University, Netherlands 0.04
Centre Hospitalier Le Mans, France 0.04
Alps Grenoble University Hospital (CHU Grenoble Alpes), France 0.03
Faculty of Medicine and Pharmacy, University of Poitiers, France 0.03
Institute for Advanced Biosciences (IAB), France 0.03
Institut du Thorax (IdT), France 0.03
CHU de Poitiers, France 0.03
UCLA David Geffen School of Medicine (DGSOM), United States of America (USA) 0.03
Oxford MRC Weatherall Institute of Molecular Medicine (WIMM), United Kingdom (UK) 0.02
Clinical Genetics Service, NUH, United Kingdom (UK) 0.02
John Radcliffe Hospital, United Kingdom (UK) 0.02
University Hospital Southampton NHS Foundation Trust, United Kingdom (UK) 0.02
Children's Hospital Colorado, United States of America (USA) 0.02
Department of Pediatrics, CU Anschutz, United States of America (USA) 0.02
Hôpital l'Archet, France 0.02
USC Children's Hospital Los Angeles (CHLA), United States of America (USA) 0.02
School of Medicine, Wayne State University, United States of America (USA) 0.02
University of Pittsburgh School of Medicine (UPSOM), United States of America (USA) 0.01
University of Pittsburgh Medical Center (UPMC), United States of America (USA) 0.01
Children's Hospital of Philadelphia (CHOP), United States of America (USA) 0.01
Institute of Human Genetics, HHU, Germany 0.01
Division of Clinical and Metabolic Genetics, SickKids U of T, Canada 0.01
UCLA Department of Human Genetics, United States of America (USA) 0.01
Toulouse University Hospital (CHU-Toulouse), France 0.01
Institute of Medical Science (IMS), U of T, Canada 0.01

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