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  • Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.

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Research Article
Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.

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    Citation

    Meindl A, Hosenfeld D, Brückl W, et al
    Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.
    Journal of Medical Genetics 1993;30:838-842.

    Publication history

    • First published October 1, 1993.
    Online issue publication 
    April 27, 2016

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