An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld–Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism

Authors

  • Feng Li,

    1. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland
    Current affiliation:
    1. Kaiser Permanente, San Jose Medical Center, San Jose, California.
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  • Denise A.S. Batista,

    1. Cytogenetics Laboratory, Kennedy Krieger Institute, Baltimore, Maryland
    2. Department of Pathology, Johns Hopkins University, Baltimore, Maryland
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  • Irene Maumenee,

    1. Department of Ophthalmology, Johns Hopkins University, Baltimore, Maryland
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  • Tao Wang

    Corresponding author
    1. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland
    • McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, 733 North Broadway, BRB513, Baltimore, MD 21205.
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  • How to Cite this Article: Li F, Batista DAS, Maumenee I, Wang T. 2010. An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld–Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism. Am J Med Genet Part A 152A:1318–1321.

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