You are here

Article info

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

Authors

    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 
    April 27, 2016

    Request permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.