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Clinical Genetics
MG-119 The evolving features of nicolaides-baraitser syndrome – a case report of a twenty-years follow-up

Authors

  • Resham Ejaz 1Department of Paediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Riyana Babul-Hirji 1Department of Paediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • David Chitayat 1Department of Paediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada2The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles

Citation

Ejaz R, Babul-Hirji R, Chitayat D
MG-119 The evolving features of nicolaides-baraitser syndrome – a case report of a twenty-years follow-up
Journal of Medical Genetics 2015;52:A5.

Publication history

  • First published December 4, 2015.
Online issue publication 
April 27, 2016

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© 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions