Differential diagnosis of Smith–Magenis syndrome: 1p36 deletion syndrome

Authors

  • Gustavo H. Vieira,

    1. J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina
    2. Department of Genetics, University of São Paulo State, Botucatu, SP, Brazil
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  • Jayson D. Rodriguez,

    1. J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina
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  • Raquel Boy,

    1. Faculty of Medical Sciences, Department of Pediatrics, State University of Rio de Janeiro, Rio de Janeiro, Brazil
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  • Isaias Soares de Paiva,

    1. Faculty of Medical Sciences, Department of Pediatrics, State University of Rio de Janeiro, Rio de Janeiro, Brazil
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  • Barbara R. DuPont,

    1. J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina
    2. Department of Genetics & Biochemistry, Clemson University, Clemson, South Carolina
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  • Danilo Moretti-Ferreira,

    Corresponding author
    1. Department of Genetics, University of São Paulo State, Botucatu, SP, Brazil
    • Department of Genetics, University of São Paulo State, Botucatu, SP, Brazil.
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  • Anand K. Srivastava

    Corresponding author
    1. J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina
    2. Department of Genetics & Biochemistry, Clemson University, Clemson, South Carolina
    • J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, 113 Gregor Mendel Circle, Greenwood, SC 29646.
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  • How to Cite this Article: Vieira GH, Rodriguez JD, Boy R, de Paiva IS, DuPont BR, Moretti-Ferreira D, Srivastava AK. 2011. Differential diagnosis of Smith–Magenis syndrome: 1p36 deletion syndrome. Am J Med Genet Part A 155:988–992.

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