Related Articles
Identification of a mutation in the WISP3 gene in three unrelated families with progressive pseudorheumatoid dysplasia
Identification of two novel mutations in the COMP gene in six families with pseudoachondroplasia
Distinct magnetic resonance imaging features in a patient with novel RARS2 mutations: A case report and review of the literature
Evaluation of the promoter region polymorphism (5‑HTTLPR) in the serotonin transporter gene in females with postpartum depression
Mild Camurati‑Engelamann disease presenting with exophthalmos as the first and only manifestation: A case report