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Open Access
Peer-reviewed
Research Article
Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria
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Samin A. Sajan,
Affiliation Department of Pediatrics, Section of Neurology, Baylor College of Medicine, Houston, Texas, United States of America
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Liliana Fernandez,
Affiliation Department of Neurology, University of California, San Francisco, San Francisco, California, United States of America
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Sahar Esmaeeli Nieh,
Affiliation Department of Neurology, University of California, San Francisco, San Francisco, California, United States of America
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Eric Rider,
Affiliation Department of Neurology, University of California, San Francisco, San Francisco, California, United States of America
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Polina Bukshpun,
Affiliation Department of Neurology, University of California, San Francisco, San Francisco, California, United States of America
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Mari Wakahiro,
Affiliation Department of Neurology, University of California, San Francisco, San Francisco, California, United States of America
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Susan L. Christian,
Affiliation Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, United States of America
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Jean-Baptiste Rivière,
Affiliation Equipe Génétique des Anomalies du Dévelopement, Université de Bourgogne, Dijon, France
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Christopher T. Sullivan,
Affiliation Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, United States of America
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Jyotsna Sudi,
Affiliation Department of Human Genetics, University of Chicago, Chicago, Illinois, United States of America
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Michael J. Herriges,
Affiliation Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America
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Alexander R. Paciorkowski,
Affiliation Departments of Neurology, Pediatrics, and Biomedical Genetics, University of Rochester Medical Center, Rochester, New York, United States of America
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A. James Barkovich,
Affiliation Department of Radiology and Biomedical Imaging, Division of Neuroradiology, University of California, San Francisco, San Francisco, California, United States of America
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Joseph T. Glessner,
Affiliation Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America
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Kathleen J. Millen,
Affiliations Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, United States of America, Department of Pediatrics, University of Washington, Seattle, Washington, United States of America
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Hakon Hakonarson,
Affiliations Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America, Department of Pediatrics, the Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America
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William B. Dobyns,
Affiliations Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, United States of America, Department of Pediatrics, University of Washington, Seattle, Washington, United States of America, Department of Neurology, University of Washington, Seattle, Washington, United States of America
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Elliott H. Sherr
* E-mail: SherrE@neuropeds.ucsf.edu
Affiliation Department of Neurology, University of California, San Francisco, San Francisco, California, United States of America
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Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria
- Samin A. Sajan,
- Liliana Fernandez,
- Sahar Esmaeeli Nieh,
- Eric Rider,
- Polina Bukshpun,
- Mari Wakahiro,
- Susan L. Christian,
- Jean-Baptiste Rivière,
- Christopher T. Sullivan,
- Jyotsna Sudi
- Published: October 3, 2013
- https://doi.org/10.1371/journal.pgen.1003823