Works matching IS 03000664 AND DT 2005 AND VI 63 AND IP 1


Results: 20
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    Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).

    Published in:
    Clinical Endocrinology, 2005, v. 63, n. 1, p. 10, doi. 10.1111/j.1365-2265.2005.02291.x
    By:
    • Turton, James P. G.;
    • Mehta, Ameeta;
    • Raza, Jamal;
    • Woods, Kathryn S.;
    • Tiulpakov, Anatoly;
    • Cassar, Joseph;
    • Chong, Kling;
    • Thomas, Paul Q.;
    • Eunice, Marumudi;
    • Ammini, Ariachery C.;
    • Bouloux, Pierre M.;
    • Starzyk, Jerzy;
    • Hindmarsh, Peter C.;
    • Dattani, Mehul T.
    Publication type:
    Article
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