Detection of <italic>SHOX</italic> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature

• मुख्य लेखकों: Semra Gürsoy (लेखक), Filiz Hazan (लेखक), Ayça Aykut (लेखक), Özlem Nalbantoğlu (लेखक), Hüseyin Anıl Korkmaz (लेखक), Korcan Demir (लेखक), Behzat Özkan (लेखक), Özgür Çoğulu (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Galenos Yayincilik, 2020-12-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: Connect to this object online.

Objective:<i>SHOX</i> 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 t...