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Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature.
Delil K, Karabulut HG, Hacıhamdioğlu B, Şıklar Z, Berberoğlu M, Öçal G, Tükün A, Ruhi HI. Delil K, et al. Among authors: hacihamdioglu b. J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):144-9. doi: 10.4274/jcrpe.2307. Epub 2015 Dec 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 26758084 Free PMC article.
Two siblings with isolated GH deficiency due to loss-of-function mutation in the GHRHR gene: successful treatment with growth hormone despite late admission and severe growth retardation.
Sıklar Z, Berberoğlu M, Legendre M, Amselem S, Evliyaoğlu O, Hacıhamdioğlu B, Savaş Erdeve S, Oçal G. Sıklar Z, et al. Among authors: hacihamdioglu b. J Clin Res Pediatr Endocrinol. 2010;2(4):164-7. doi: 10.4274/jcrpe.v2i4.164. Epub 2010 Nov 6. J Clin Res Pediatr Endocrinol. 2010. PMID: 21274317 Free PMC article.
51 results