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Genome-wide assessment of the association of rare and common copy number variations to testicular germ cell cancer.
Edsgärd D, Dalgaard MD, Weinhold N, Wesolowska-Andersen A, Rajpert-De Meyts E, Ottesen AM, Juul A, Skakkebæk NE, Skøt Jensen T, Gupta R, Leffers H, Brunak S. Edsgärd D, et al. Among authors: ottesen am. Front Endocrinol (Lausanne). 2013 Jan 29;4:2. doi: 10.3389/fendo.2013.00002. eCollection 2013. Front Endocrinol (Lausanne). 2013. PMID: 23372565 Free PMC article.
Heterozygous deletion at the RLN1 locus in a family with testicular germ cell cancer identified by integrating copy number variation data with phenome and interactome information.
Edsgärd D, Scheel M, Hansen NT, Ralfkiaer U, Jensen TS, Skakkebaek NE, Brunak S, Gupta R, Rajpert-De Meyts E, Ottesen AM. Edsgärd D, et al. Among authors: ottesen am. Int J Androl. 2011 Aug;34(4 Pt 2):e122-32. doi: 10.1111/j.1365-2605.2011.01188.x. Epub 2011 Jun 22. Int J Androl. 2011. PMID: 21696394
21 results