Søgeresultater - M I New

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

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

    Udgivet 1988
    Få fuldtekst
    Artigo
    Føj til favoritter
    Saved in:
  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. af Grace M. Tannin, Ameeta K. Agarwal, Carl Monder, M I New, P.C. White

    Udgivet 1991
    Få fuldtekst
    Artigo
    Føj til favoritter
    Saved in:
  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. af Perrin C. White, Jakob Dupont, M I New, E Leiberman, Ze’ev Hochberg, Ariel Rösler

    Udgivet 1991
    Få fuldtekst Få fuldtekst
    Artigo
    Føj til favoritter
    Saved in:
  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. af Leigh Pascoe, Kathleen M. Curnow, Liliya Slutsker, J Connell, Phyllis Speiser, M I New, Perrin C. White

    Udgivet 1992
    Få fuldtekst
    Artigo
    Føj til favoritter
    Saved in:

Søgeredskaber: