| Authors: |
Young RE; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA., Qiao L; Department of Pediatrics, Columbia University Irving Medical Center, New York, New York, USA.; Department of Systems Biology, Columbia University Irving Medical Center, New York, New York, USA., Hernan R; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA., Sweetser DA; Division of Medical Genetics and Metabolism, Department of Pediatrics; and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA., Waxler JL; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA., Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Scott TM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Azamian MS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Bostwick B; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Burrage LC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA., Rodan LH; Division of Genetics and Genomics and Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA., Russell BE; Department of Human Genetics, Division of Clinical Genetics, Department of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, California, USA., Dutra-Clarke M; Department of Human Genetics, Division of Clinical Genetics, Department of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, California, USA., Kruer M; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, Arizona, USA.; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona, USA., Bakhtiarim S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, Arizona, USA.; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona, USA., Darvish H; Neuroscience Research Center, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran., Amor DJ; Murdoch Children's Research Institute and University of Melbourne Department of Paediatrics, Royal Children's Hospital, Melbourne, Australia., Rahman S; Mitochondrial Research Group, UCL Great Ormond Street Institute of Child Health, and Metabolic Department, Great Ormond Street Hospital for Children, London, UK., Stals K; Exeter Genomics Laboratory, Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK., Bradley L; Department of Clinical Genetics and Department of Neurology, Children's Health Ireland (CHI) at Crumlin, Dublin, Ireland., Byrne S; Department of Clinical Genetics and Department of Neurology, Children's Health Ireland (CHI) at Crumlin, Dublin, Ireland., Tolusso LK; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Wong B; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Benedict L; Center for Human Genetics, University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA., Wallis K; Center for Human Genetics, University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA., Micke K; Colorado Fetal Care Center, Children's Hospital Colorado, Aurora, Colorado, USA., Colson C; Univ. Lille, CHU Lille, ULR7364-RADEME-Maladies RAres du DEveloppement Embryonnaire et du Métabolisme, CRMR Anomalies du Développement et Syndromes Malformatifs, Lille, France., Smol T; Univ. Lille, CHU Lille, ULR7364-RADEME-Maladies RAres du DEveloppement Embryonnaire et du Métabolisme, CRMR Anomalies du Développement et Syndromes Malformatifs, Lille, France., Southwick SV; Division of Maternal Fetal Medicine, Department of Gynecology and Obstetrics, Johns Hopkins Hospital, Baltimore, Maryland, USA., Miller KA; Division of Maternal Fetal Medicine, Department of Gynecology and Obstetrics, Johns Hopkins Hospital, Baltimore, Maryland, USA., Kush ML; Center for Fetal Therapy, Department of Gynecology & Obstetrics, Johns Hopkins University, Baltimore, Maryland, USA., Chorin O; Institute of Rare Diseases, Edmond and Lily Safra Hospital for Children, the Danek Gertner Institute of Genetics, Sheba Medical Center, Ramat Gan, Israel., Rothschild A; Institute of Rare Diseases, Edmond and Lily Safra Hospital for Children, the Danek Gertner Institute of Genetics, Sheba Medical Center, Ramat Gan, Israel., Wang W; GeneDx, LLC, Gaithersburg, Maryland, USA., Shen Y; Department of Systems Biology, Columbia University Irving Medical Center, New York, New York, USA.; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, New York, USA.; JP Sulzberger Columbia Genome Center, Columbia University Irving Medical Center, New York, New York, USA., Chung WK; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA. |
