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The complex craniofacial signature of fibrodysplasia ossificans progressiva: Whose handwriting is it?

Authors

  • Peter Hammond,

    Corresponding author
    1. Molecular Medicine Unit, UCL Institute of Child Health, London, UK
    • Professor, Molecular Medicine Unit, UCL Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK
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  • Michael Suttie,

    1. Molecular Medicine Unit, UCL Institute of Child Health, London, UK
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  • Raoul C. Hennekam,

    1. Department of Pediatrics, AMC, University of Amsterdam, Amsterdam, The Netherlands
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  • Judith Allanson,

    1. Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada
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  • Eileen M. Shore,

    1. Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, Pennsylvania
    2. Department of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania
    3. Center for Research in FOP and Related Disorders, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania
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  • Frederick S. Kaplan

    1. Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, Pennsylvania
    2. Center for Research in FOP and Related Disorders, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania
    3. Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania
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  • How to Cite this Article: Hammond P, Suttie M, Hennekam RC, Allanson J, Shore EM, Kaplan FS. 2012. The complex craniofacial signature of fibrodysplasia ossificans progressiva: Whose handwriting is it? Am J Med Genet Part A 158A: 2979–2980.

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