Authors: Fluck, CE Deladoey, J Nayak, S Zeller, O Kopp, P Mullis, PE

Citation: Ce. Fluck et al., Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59 Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II), EUR J ENDOC, 145(4), 2001, pp. 439-444

Authors: Vuissoz, JM Deladoey, J Buyukgebiz, A Cemeroglu, P Gex, G Gallati, S Mullis, PE

Citation: Jm. Vuissoz et al., New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism, J CLIN END, 86(9), 2001, pp. 4468-4471

Authors: Deladoey, J Stocker, P Mullis, PE

Citation: J. Deladoey et al., Autosomal dominant GH deficiency due to an Arg(183)His GH-1 gene mutation:Clinical and molecular evidence of impaired regulated GH secretion, J CLIN END, 86(8), 2001, pp. 3941-3947

Authors: Nuoffer, JM Fluck, C Deladoey, J Eble, A Dattani, MT Mullis, PE

Citation: Jm. Nuoffer et al., Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line, J ENDOCR, 165(2), 2000, pp. 313-320

Authors: Deladoey, J Fluck, C Buyukgebiz, A Kuhlmann, BV Eble, A Hindmarsh, PC Wu, W Mullis, PE

Citation: J. Deladoey et al., "Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency, J CLIN END, 84(5), 1999, pp. 1645-1650

Authors: Deladoey, J Fluck, C Bex, M Yoshimura, N Harada, N Mullis, PE

Citation: J. Deladoey et al., Aromatase deficiency caused by a novel P450(arom) gene mutation: Impact ofabsent estrogen production on serum gonadotropin concentration in a boy, J CLIN END, 84(11), 1999, pp. 4050-4054