Current Concepts Review - Update on the Genetic Bases of Disorders with Orthopaedic Manifestations*
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Orthopedics and Sports Medicine,General Medicine,Surgery
Reference94 articles.
1. The frequency of patients with dystrophin abnormalities in a limb-girdle patient population
2. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
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5. The Treatment of Cleidocranial Dysostosis (Scheuthauer-Marie-Sainton Syndrome), a Rare Form of Skeletal Dysplasia, Accompanied by Spinal Deformities: A Review of the Literature and Two Case Reports;Case Reports in Orthopedics;2018-07-09
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