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Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome

  • Jill A. Rosenfeld,

    Affiliation Signature Genomic Laboratories, LLC, Spokane, Washington, United States of America

  • Blake C. Ballif,

    Affiliation Signature Genomic Laboratories, LLC, Spokane, Washington, United States of America

  • Ann Lucas,

    Affiliation Carolinas Medical Center, Clinical Genetics Center, Charlotte, North Carolina, United States of America

  • Edward J. Spence,

    Affiliation Carolinas Medical Center, Clinical Genetics Center, Charlotte, North Carolina, United States of America

  • Cynthia Powell,

    Affiliation Departments of Pediatrics and Genetics, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, United States of America

  • Arthur S. Aylsworth,

    Affiliation Departments of Pediatrics and Genetics, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, United States of America

  • Beth A. Torchia,

    Affiliation Signature Genomic Laboratories, LLC, Spokane, Washington, United States of America

  • Lisa G. Shaffer

    shaffer@signaturegenomics.com

    Affiliation Signature Genomic Laboratories, LLC, Spokane, Washington, United States of America

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