• A Novel Intronic Splicing Mutation in the <em>EXT2</em> Gene of a Chinese Family with Multiple Osteochondroma
• A Novel Intronic Splicing Mutation in the EXT2 Gene of a Chinese Family with Multiple Osteochondroma
• A novel splice mutation induces exon skipping of the EXT1 gene in patients with hereditary multiple exostoses
• A patient with pseudohypoparathyroidism type 1A previously misdiagnosed as hereditary multiple exostosis: A case report
• Clinical and Functional Outcomes of Ulnar Lengthening in the Treatment of Masada Type I Forearm Deformities in Hereditary Multiple Osteochondromas
• Factors influencing postoperative bleeding after dental extraction in older adult patients receiving anticoagulation therapy
• Gradual ulnar lengthening in Masada type I/IIb deformity in patients with hereditary multiple osteochondromas: a retrospective study with a mean follow-up of 4.2 years
• Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family
• Identification of risk factors affecting bone formation in gradual ulnar lengthening in children with hereditary multiple exostoses: A retrospective study
• Mixed Phenotype of Langer-Giedion's and Cornelia de Lange's Syndromes in an 8q23.3-q24.1 Microdeletion without <em>TRPS1</em> Deletion
• Mixed Phenotype of Langer-Giedion's and Cornelia de Lange's Syndromes in an 8q23.3-q24.1 Microdeletion without TRPS1 Deletion
• Modified ulnar lengthening for correction of the Masada type 2 forearm deformity in hereditary multiple exostosis
• Mutational Analysis of <em>EXT1</em>in a Chinese Family Affected by Hereditary Multiple Osteochondroma
• Mutational Analysis of EXT1in a Chinese Family Affected by Hereditary Multiple Osteochondroma
• Natural History and Characteristics of Hand Exostoses in Multiple Hereditary Exostoses
• Older age and multi-joint external fixator are two risk factors of complications in ulnar lengthening in children with hereditary multiple exostosis
• Single-Bone Forearm as a Salvage Procedure in Recalcitrant Pediatric Forearm Pathologies
• The One-Bone Forearm in Children: Surgical Technique and a Retrospective Review of Outcomes
• Total hip arthroplasty in hereditary multiple exostosis patients: literature review and evaluation of 10 cases
• Whole-exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family
• Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family