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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Detalles Bibliográficos
Autores principales: Alharthi, Abdulla A., El-Hallous, Ehab I., Talaat, Iman M., Alghamdi, Hamed A., Almalki, Matar I., Gaber, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687980/
https://www.ncbi.nlm.nih.gov/pubmed/29158767
http://dx.doi.org/10.3345/kjp.2017.60.10.327

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687980/
https://www.ncbi.nlm.nih.gov/pubmed/29158767
http://dx.doi.org/10.3345/kjp.2017.60.10.327

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