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  • Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications

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Neurogenetics
Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications

Authors

  • Fátima Torres CGC Genetics, Porto, Portugal Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Porto, Portugal PubMed articlesGoogle scholar articles
  • Mafalda Barbosa Department of Genetics and Genomic Sciences, The Mindich Child Health & Development Institute, The Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, USA Instituto Gulbenkian de Ciência, Oeiras, Portugal PubMed articlesGoogle scholar articles
  • Patrícia Maciel Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal ICVS/3B's—PT Government Associate Laboratory, Braga/Guimarães, Portugal PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Patrícia Maciel, Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, 4710-057 Braga, Portugal; pmaciel{at}ecsaude.uminho.pt
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Citation

Torres F, Barbosa M, Maciel P
Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications
Journal of Medical Genetics 2016;53:73-90.

Publication history

  • Received August 11, 2015
  • Revised September 27, 2015
  • Accepted September 28, 2015
  • First published October 26, 2015.
Online issue publication 
April 27, 2016

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