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Developmental disability and hypomelanosis of Ito in a female with 7.3 Mb de novo duplication of Xp11.3-p11.4 and random X inactivation

Authors

  • Ying S. Zou,

    1. Center for Human Genetics, Boston University School of Medicine, Boston, Massachusetts
    2. Department of Pediatrics, Boston University School of Medicine, Boston, Massachusetts
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  • Jeff M. Milunsky

    Corresponding author
    1. Center for Human Genetics, Boston University School of Medicine, Boston, Massachusetts
    2. Department of Pediatrics, Boston University School of Medicine, Boston, Massachusetts
    3. Department of Genetics and Genomics, Boston University School of Medicine, Boston, Massachusetts
    • Center for Human Genetics, Boston University School of Medicine, Boston, MA 02118.
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  • How to cite this article: Zou YS, Milunsky JM. 2009. Developmental disability and hypomelanosis of Ito in a female with 7.3 Mb de novo duplication of Xp11.3-p11.4 and random X inactivation. Am J Med Genet Part A 149A:2573–2577.

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