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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Detalles Bibliográficos
Autores principales: Delil, Kenan, Karabulut, Halil Gürhan, Hacıhamdioğlu, Bülent, Şıklar, Zeynep, Berberoğlu, Merih, Öçal, Gönül, Tükün, Ajlan, Ruhi, Hatice Ilgın
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096468/
https://www.ncbi.nlm.nih.gov/pubmed/26758084
http://dx.doi.org/10.4274/jcrpe.2307

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096468/
https://www.ncbi.nlm.nih.gov/pubmed/26758084
http://dx.doi.org/10.4274/jcrpe.2307

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