Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature

OBJECTIVE: SHOX gene mutations constitute one of the genetic causes of short stature. The clinical phenotype includes variable degrees of growth impairment, such as Langer mesomelic dysplasia (LMD), Léri-Weill dyschondrosteosis (LWD) or idiopathic short stature (ISS). The aim of this study was to de...

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Detalles Bibliográficos
Autores principales: Gürsoy, Semra, Hazan, Filiz, Aykut, Ayça, Nalbantoğlu, Özlem, Korkmaz, Hüseyin Anıl, Demir, Korcan, Özkan, Behzat, Çoğulu, Özgür
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711637/
https://www.ncbi.nlm.nih.gov/pubmed/32295321
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2019.0001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711637/
https://www.ncbi.nlm.nih.gov/pubmed/32295321
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2019.0001

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