Center-Authored Papers

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Filters: Author is Tapscott, Stephen [Clear All Filters]

2013

Marotta M, Chen X, Watanabe T, Faber PW, Diede SJ, Tapscott S, Tubbs R, Kondratova A, Stephens R, Tanaka H. 2013. Homology-mediated end-capping as a primary step of sister chromatid fusion in the breakage-fusion-bridge cycles.. Nucleic acids research. Abstract

2015

Lemmers RJLF, van den Boogaard ML, van der Vliet PJ, Donlin-Smith CM, Nations SP, Ruivenkamp CAL, Heard P, Bakker B, Tapscott S, Cody JD et al.. 2015. Hemizygosity for SMCHD1 in Facioscapulohumeral Muscular Dystrophy Type 2: Consequences for 18p Deletion Syndrome.. Human mutation. Abstract

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