Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family. [PDF]
Li Y, Lin X, Zhu M, Li J, Yuan Z, Xu H.
europepmc +1 more source
What\u27s new in orthopaedic research [PDF]
Sandell, Linda J., Silva, Matthew J.
core +1 more source
Total Hip Arthroplasty for Secondary Coxarthrosis in Patients with Hereditary Multiple Exostoses: Minimum 5-Year Follow-up Results and Surgical Considerations. [PDF]
Yoon JY +4 more
europepmc +1 more source
Novel deletion and 2397 G>T mutations of the EXT1 gene identified in two Chinese pedigrees with hereditary multiple exostoses using exon sequencing. [PDF]
Shen Y +5 more
europepmc +1 more source
Total hip arthroplasty in hereditary multiple exostoses with secondary osteoarthritis: A case report. [PDF]
Kim WJ +10 more
europepmc +1 more source
Malignant Progression in Two Children with Multiple Osteochondromas [PDF]
Gregory A. Schmale +3 more
core +1 more source
Hereditary multiple exostoses: are there new plausible treatment strategies? [PDF]
Pacifici M.
europepmc +1 more source

