Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma

Chordoma is a rare bone cancer that is believed to originate from notochordal remnants. We previously identified germline T duplication as a major susceptibility mechanism in several chordoma families. Recently, a common genetic variant in T (rs2305089) was significantly associated with the risk of...

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Bibliografiset tiedot
Julkaisussa:Hum Genet
Päätekijät: Kelley, MJ, Shi, J, Ballew, B, Hyland, PL, Li, WQ, Rotunno, M, Alcorta, DA, Liebsch, NJ, Mitchell, J, Bass, S, Roberson, D, Boland, J, Cullen, M, He, J, Burdette, L, Yeager, M, Chanock, SJ, Parry, DM, Goldstein, AM, Yang, XR
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2014
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6938388/
https://ncbi.nlm.nih.gov/pubmed/24990759
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-014-1463-z
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