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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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Dettagli Bibliografici
Pubblicato in:J Clin Res Pediatr Endocrinol
Autori principali: Delil, Kenan, Karabulut, Halil Gürhan, Hacıhamdioğlu, Bülent, Şıklar, Zeynep, Berberoğlu, Merih, Öçal, Gönül, Tükün, Ajlan, Ruhi, Hatice Ilgın
Natura: Artigo
Lingua:Inglês
Pubblicazione: Galenos Publishing 2016
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Accesso online: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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