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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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| 出版年: | J Clin Res Pediatr Endocrinol |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Galenos Publishing
2016
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| 主題: | |
| オンライン･アクセス: | 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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