Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability

• Christina Grau ,

  Contributed equally to this work with: Christina Grau, Molly Starkovich

  Affiliation Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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• Molly Starkovich ,

  Contributed equally to this work with: Christina Grau, Molly Starkovich

  Affiliation Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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• Mahshid S. Azamian,

  Affiliation Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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• Fan Xia,

  Affiliations Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America, Baylor Genetics, Houston, Texas, Unite States of America

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• Sau Wai Cheung,

  Affiliations Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America, Baylor Genetics, Houston, Texas, Unite States of America

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• Patricia Evans,

  Affiliation Departments of Pediatrics and Neurology, University of Texas Southwestern Medical School, Dallas, Texas, United States of America

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• Alex Henderson,

  Affiliation The Newcastle upon Tyne Hospitals, Newcastle upon Tyne, England

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• Seema R. Lalani,

  Affiliation Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America

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• Daryl A. Scott

  * E-mail: dscott@bcm.edu

  Affiliations Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America, Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, United States of America

  http://orcid.org/0000-0003-1460-5169

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