Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature

OBJECTIVE: The frequency of mutations in the short stature homeobox (SHOX) gene in patients with idiopathic short stature (ISS) ranges widely, depending mostly on the mutation detection technique and inclusion criteria. We present phenotypic and genotypic data on 38 Turkish patients with ISS and the...

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書目詳細資料
發表在:J Clin Res Pediatr Endocrinol
Main Authors: Delil, Kenan, Karabulut, Halil Gürhan, Hacıhamdioğlu, Bülent, Şıklar, Zeynep, Berberoğlu, Merih, Öçal, Gönül, Tükün, Ajlan, Ruhi, Hatice Ilgın
格式: Artigo
語言:Inglês
出版: Galenos Publishing 2016
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Original Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC5096468/
https://ncbi.nlm.nih.gov/pubmed/26758084
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.2307
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