Works matching IS 08044643 AND DT 2018 AND VI 178 AND IP 2


Results: 12
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    Next-generation panel sequencing identifies NF1 germline mutations in three patients with pheochromocytoma but no clinical diagnosis of neurofibromatosis type 1.

    Published in:
    European Journal of Endocrinology, 2018, v. 178, n. 2, p. K1, doi. 10.1530/EJE-17-0714
    By:
    • Gieldon, Laura;
    • Masjkur, Jimmy Rusdian;
    • Richter, Susan;
    • Därr, Roland;
    • Lahera, Marcos;
    • Aust, Daniela;
    • Zeugner, Silke;
    • Rump, Andreas;
    • Hackmann, Karl;
    • Tzschach, Andreas;
    • Januszewicz, Andrzej;
    • Prejbisz, Aleksander;
    • Eisenhofer, Graeme;
    • Schrock, Evelin;
    • Robledo, Mercedes;
    • Klink, Barbara
    Publication type:
    Article
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