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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Bibliografische gegevens
Gepubliceerd in:J Clin Res Pediatr Endocrinol
Hoofdauteurs: Delil, Kenan, Karabulut, Halil Gürhan, Hacıhamdioğlu, Bülent, Şıklar, Zeynep, Berberoğlu, Merih, Öçal, Gönül, Tükün, Ajlan, Ruhi, Hatice Ilgın
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Galenos Publishing 2016
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Original Article
Online toegang: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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