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Cytogenetics/Microarray and Molecular Genetics
MG-138 Co-occurrence of cohen syndrome with 16p11.2 duplication: The exome sequencing approach

Authors

  • Jila Dastan 1Department of Medical Genetics, University of BC, Vancouver, British Columbia, Canada4BC Child and Family Research Institute, University of BC, Vancouver, British Columbia, Canada5Children’s and Women’s Health Center of BC, University of British Columbia, Vancouver, British Columbia, Canada PubMed articlesGoogle scholar articles
  • Flamingo Tang 2Department of Pathology and Lab Medicine, University of BC, Vancouver, British Columbia, Canada4BC Child and Family Research Institute, University of BC, Vancouver, British Columbia, Canada5Children’s and Women’s Health Center of BC, University of British Columbia, Vancouver, British Columbia, Canada PubMed articlesGoogle scholar articles
  • Ying Qiao 1Department of Medical Genetics, University of BC, Vancouver, British Columbia, Canada2Department of Pathology and Lab Medicine, University of BC, Vancouver, British Columbia, Canada4BC Child and Family Research Institute, University of BC, Vancouver, British Columbia, Canada5Children’s and Women’s Health Center of BC, University of British Columbia, Vancouver, British Columbia, Canada PubMed articlesGoogle scholar articles
  • Chieko Chijiwa 1Department of Medical Genetics, University of BC, Vancouver, British Columbia, Canada3Provincial Medical Genetics Program, University of BC, Vancouver, British Columbia, Canada5Children’s and Women’s Health Center of BC, University of British Columbia, Vancouver, British Columbia, Canada PubMed articlesGoogle scholar articles
  • Kristina Calli 1Department of Medical Genetics, University of BC, Vancouver, British Columbia, Canada4BC Child and Family Research Institute, University of BC, Vancouver, British Columbia, Canada5Children’s and Women’s Health Center of BC, University of British Columbia, Vancouver, British Columbia, Canada PubMed articlesGoogle scholar articles
  • Evica Rajcan-Separovic 1Department of Medical Genetics, University of BC, Vancouver, British Columbia, Canada2Department of Pathology and Lab Medicine, University of BC, Vancouver, British Columbia, Canada4BC Child and Family Research Institute, University of BC, Vancouver, British Columbia, Canada5Children’s and Women’s Health Center of BC, University of British Columbia, Vancouver, British Columbia, Canada PubMed articlesGoogle scholar articles
  • Suzanne ME Lewis 1Department of Medical Genetics, University of BC, Vancouver, British Columbia, Canada3Provincial Medical Genetics Program, University of BC, Vancouver, British Columbia, Canada4BC Child and Family Research Institute, University of BC, Vancouver, British Columbia, Canada5Children’s and Women’s Health Center of BC, University of British Columbia, Vancouver, British Columbia, Canada PubMed articlesGoogle scholar articles

Citation

Dastan J, Tang F, Qiao Y, et al
MG-138 Co-occurrence of cohen syndrome with 16p11.2 duplication: The exome sequencing approach
Journal of Medical Genetics 2015;52:A10-A11.

Publication history

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

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