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PubMed (OMIM) for id: 121775

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A common single-nucleotide variant in T is strongly associated with chordoma.
Pillay N, Plagnol V, Tarpey PS, Lobo SB, Presneau N, Szuhai K, Halai D, Berisha F, Cannon SR, Mead S, Kasperaviciute D, Palmen J, Talmud PJ, Kindblom LG, Amary MF, Tirabosco R, Flanagan AM. Pillay N, et al. Nat Genet. 2012 Nov;44(11):1185-7. doi: 10.1038/ng.2419. Epub 2012 Oct 14. Nat Genet. 2012. PMID: 23064415
Chordoma in siblings.
FOOTE RF, ABLIN G, HALL WW. FOOTE RF, et al. Calif Med. 1958 May;88(5):383-6. Calif Med. 1958. PMID: 13523418 Free PMC article. No abstract available.
Familial chordoma with probable autosomal dominant inheritance.
Stepanek J, Cataldo SA, Ebersold MJ, Lindor NM, Jenkins RB, Unni K, Weinshenker BG, Rubenstein RL. Stepanek J, et al. Am J Med Genet. 1998 Jan 23;75(3):335-6. doi: 10.1002/(sici)1096-8628(19980123)75:3<335::aid-ajmg23>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9475610 No abstract available.