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Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.
Srivastava, Siddharth; Love-Nichols, Jamie A; Dies, Kira A; Ledbetter, David H; Martin, Christa L; Chung, Wendy K; Firth, Helen V; Frazier, Thomas; Hansen, Robin L; Prock, Lisa; Brunner, Han; Hoang, Ny; Scherer, Stephen W; Sahin, Mustafa; Miller, David T.
Affiliation
  • Srivastava S; Translational Neuroscience Center, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Love-Nichols JA; Translational Neuroscience Center, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Dies KA; Translational Neuroscience Center, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Ledbetter DH; Autism & Developmental Medicine Institute, Geisinger, Danville, PA, USA.
  • Martin CL; Autism & Developmental Medicine Institute, Geisinger, Danville, PA, USA.
  • Chung WK; Departments of Pediatrics and Medicine, Columbia University, New York, NY, USA.
  • Firth HV; SFARI, Simons Foundation, New York, NY, USA.
  • Frazier T; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
  • Hansen RL; East Anglian Medical Genetics Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, UK.
  • Prock L; Autism Speaks, Cleveland, OH, USA.
  • Brunner H; MIND Institute, Department of Pediatrics, University of California Davis, Sacramento, CA, USA.
  • Hoang N; Translational Neuroscience Center, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Scherer SW; Developmental Medicine Center, Boston Children's Hospital, Boston, MA, USA.
  • Sahin M; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Miller DT; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
Genet Med ; 22(10): 1731-1732, 2020 Oct.
Article in En | MEDLINE | ID: mdl-32728138
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Systematic_reviews Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Systematic_reviews Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: