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  1. 1
    Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

    Characterization of frequent deletions causing steroid 21-hydroxylase deficiency. 由 Perrin C. White, A Vitek, Bo Dupont, M I New

    出版 1988
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  2. 2
    The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization.

    The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization. 由 Grace M. Tannin, Ameeta K. Agarwal, Carl Monder, M I New, P.C. White

    出版 1991
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  3. 3
    A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin.

    A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin. 由 Perrin C. White, Jakob Dupont, M I New, E Leiberman, Ze’ev Hochberg, Ariel Rösler

    出版 1991
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  4. 4
    Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2.

    Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2. 由 Leigh Pascoe, Kathleen M. Curnow, Liliya Slutsker, J Connell, Phyllis Speiser, M I New, Perrin C. White

    出版 1992
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