• 15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature
• A case report of acampomelic campomelic dysplasia and operative difficulties in cleft palate reconstruction
• Brachymetatarsia: A Classification for Surgical Treatment
• Constant inhibition in congenital lower extremity shortening: does it begin in utero?
• Dentoalveolar Abscesses Not Associated with Caries or Trauma: A Diagnostic Hallmark of Hypophosphatemic Rickets Initially Misdiagnosed as Hypochondroplasia
• Early clinical and radiological improvement in a young boy with metaphyseal anadysplasia type 2
• Hip Dysplasia in Children With Osteogenesis Imperfecta: Association With Collagen Type I C-Propeptide Mutations
• Imaging features of lower limb malformations above the foot
• Maxillofacial Changes in Melnick-Needles Syndrome
• Natural history and genetic spectrum of the Turkish metaphyseal dysplasia cohort, including rare types caused by biallelic COL10A1, COL2A1, and LBR variants
• Nonsense mutations in FZD2 cause autosomal-dominant omodysplasia: Robinow syndrome-like phenotypes
• NOTCH2 related disorders: Description and review of the fetal presentation
• Radiological and histopathological features of short rib-polydactyly syndrome type III and identification of two novel DYNC2H1 variants
• Radiological and histopathological features of short rib‑polydactyly syndrome type III and identification of two novel <em>DYNC2H1</em> variants
• Simultaneous bilateral correction of genu varum with Smart frame
• The vascular origins of antero-medial tibial bowing in congenital fibular deficiency