Works matching IS 03000664 AND DT 2010 AND VI 73 AND IP 5


Results: 21
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    Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism.

    Published in:
    Clinical Endocrinology, 2010, v. 73, n. 5, p. 671, doi. 10.1111/j.1365-2265.2010.03849.x
    By:
    • Cangul, Hakan;
    • Morgan, Neil V.;
    • Forman, Julia R.;
    • Saglam, Halil;
    • Aycan, Zehra;
    • Yakut, Tahsin;
    • Gulten, Tuna;
    • Tarim, Omer;
    • Bober, Ece;
    • Cesur, Yasar;
    • Kirby, Gail A.;
    • Pasha, Shanaz;
    • Karkucak, Mutlu;
    • Eren, Erdal;
    • Cetinkaya, Semra;
    • Bas, Veysel;
    • Demir, Korcan;
    • Yuca, Sevil A.;
    • Meyer, Esther;
    • Kendall, Michaela
    Publication type:
    Article
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