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. [PDF]
Li Y, Wang Z, Chen M, Cai H.
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Sarcomatous Transformation of Recurrent Scapular Osteochondroma in a Patient with the Hereditary Multiple Osteochondromas: A Case Report and Literature Review. [PDF]
Sajid S +4 more
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A novel EXT2 frameshift mutation identified in a family with multiple osteochondromas. [PDF]
Chen Z, Bi Q, Kong M, Cao L, Ruan W.
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Bone sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [PDF]
Athanasou, N. +16 more
core
Analysis of mutations in EXT1 and EXT2 in Brazilian patients with multiple osteochondromas. [PDF]
Santos SCL +5 more
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Heterogeneous spectrum of EXT gene mutations in Chinese patients with hereditary multiple osteochondromas. [PDF]
Li Y +8 more
europepmc +1 more source
RNA-Seq detects a SAMD12-EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas. [PDF]
Oliver GR +12 more
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