A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate. [PDF]
Xian C +12 more
europepmc +1 more source
An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 [PDF]
core +1 more source
The roles of ext1 and ext2 in heparan sulfate polymerization and hereditary multiple exostoses
Craig McCormick
openalex +1 more source
Development of a prediction model for lower limb deformity in patients with hereditary multiple exostoses based on interpretable models and nomogram. [PDF]
Lu R +7 more
europepmc +1 more source
Endoscopic endonasal extreme far-medial approach for a lower clivus osteochondroma in a patient with hereditary multiple exostoses: illustrative case. [PDF]
Morinaga Y +7 more
europepmc +1 more source
Multiple exostoses and an osteochondroma in a Pliocene canid from Langebaanweg 'E' Quarry (South Africa). [PDF]
Chinsamy A, Valenciano A.
europepmc +1 more source
Case of Multiple Exostoses [PDF]
openaire +2 more sources
A Rare Case of Hereditary Multiple Exostoses in a Woman. [PDF]
Ghamri RA.
europepmc +1 more source

