3 results for author:"Yordam N." in Literature citations
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| Novel splice site mutation in the growth hormone receptor gene in Turkish patients with Laron-type dwarfism. Arman A., Ozon A., Isguven P.S., Coker A., Peker I., Yordam N. J. Pediatr. Endocrinol. Metab. 21:47-58(2008) · Mapped (4) |
| Influence of iodine supplementation on serum insulin-like growth factor-I (IGF-I) and IGF-binding protein-3 (IGFBP-3) levels in severe iodine deficiency. Ozon A., Alikasifoglu A., Yordam N. Turk. J. Pediatr. 46:303-308(2004) · Mapped (24) |
| Nine novel growth hormone receptor gene mutations in patients with Laron syndrome. Sobrier M.-L., Dastot F., Duquesnoy P., Kandemir N., Yordam N., Goossens M., Amselem S. J. Clin. Endocrinol. Metab. 82:435-437(1997) · UniProtKB (1) |