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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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| Publié dans: | J Clin Res Pediatr Endocrinol |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Galenos Publishing
2016
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| Sujets: | |
| Accès en ligne: | 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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