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Research Article
Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing.
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    Citation

    Rumsby G, Massoud AF, Avey C, et al
    Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing.
    Journal of Medical Genetics 1996;33:798-799.

    Publication history

    • First published September 1, 1996.
    Online issue publication 
    September 01, 1996

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