Works matching IS 09538194 AND DT 2018 AND VI 30 AND IP 12


Results: 7
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    A novel GNRHR gene mutation causing congenital hypogonadotrophic hypogonadism in a Brazilian kindred.

    Published in:
    Journal of Neuroendocrinology, 2018, v. 30, n. 12, p. N.PAG, doi. 10.1111/jne.12658
    By:
    • Correa‐Silva, Silvia Regina;
    • Fausto, Jessica da Silva;
    • Kizys, Marina Malta Letro;
    • Filipelli, Rafael;
    • Marco Antonio, David Santos;
    • Oku, Andre Yuji;
    • Furuzawa, Gilberto Koiti;
    • Orchard, Eugenia Verônica Hernandez;
    • Costa‐Barbosa, Flavia Amanda;
    • Mitne‐Neto, Miguel;
    • Dias‐da‐Silva, Magnus R.
    Publication type:
    Article
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    Issue Information.

    Published in:
    Journal of Neuroendocrinology, 2018, v. 30, n. 12, p. N.PAG, doi. 10.1111/jne.12527
    Publication type:
    Article