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Screening of SHOX gene sequence variants in Saudi Arabian children with idiopathic short stature
PURPOSE: Short stature affects approximately 2%–3% of children, representing one of the most frequent disorders for which clinical attention is sought during childhood. Despite assumed genetic heterogeneity, mutations or deletions in the short stature homeobox-containing gene (SHOX) are frequently d...
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| Publicado no: | Korean J Pediatr |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Korean Pediatric Society
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5687980/ https://ncbi.nlm.nih.gov/pubmed/29158767 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2017.60.10.327 |
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