Osteochondroma
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-28315-5_21
Reference8 articles.
1. Bridge JA, Nelson M, Orndal C, Bhatia P, Neff JR. Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12(EXT2) in patients with sporadic and hereditary osteochondromas. Cancer. 1998;82:1657–63.
2. Ciavarella M, Coco M, Baorda F, Stanziale P, Chetta M, Bisceglia L, et al. 20 novel point mutations and one large deletion in EXT1 and EXT2 genes: report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis. Gene. 2013;515:339–48.
3. Ge X, Tsang K, He L, Garcia RA, Ermann J, Mizoguchi F, et al. NFAT restricts osteochondroma formation from entheseal progenitors. JCI Insight. 2016;1:e86254.
4. Jones KB, Piombo V, Searby C, Kurriger G, Yang B, Grabellus F, et al. A mouse model of osteochondromagenesis from clonal inactivation of Ext1 in chondrocytes. Proc Natl Acad Sci U S A. 2010;107:2054–9.
5. Mertens F, Rydholm A, Kreicbergs A, Willén H, Jonsson K, Heim S, et al. Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses. Genes Chromosomes Cancer. 1994;9:8–12.
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