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Sanchis-Juan, Alba and Stephens, Jonathan and French, Courtney E and Gleadall, Nicholas and Mégy, Karyn and Penkett, Christopher and Shamardina, Olga and Stirrups, Kathleen and Delon, Isabelle and Dewhurst, Eleanor and Dolling, Helen and Erwood, Marie and Grozeva, Detelina and Stefanucci, Luca and Arno, Gavin and Webster, Andrew R and Cole, Trevor and Austin, Topun and Branco, Ricardo Garcia and Ouwehand, Willem H and Raymond, F Lucy and Carss, Keren J (2018) Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing. Genome medicine, 10 (1). p. 95. ISSN 1756-994X. This article is available to all UHB staff and students via ASK Discovery tool http://tinyurl.com/z795c8c by using their UHB Athens login IDs
