Showing 1 - 2 results of 2 for search 'Fiona M. Robertson', query time: 0.02s Refine Results
  1. 1
    Lineage-specific rediploidization is a mechanism to explain time-lags between genome duplication and evolutionary diversification

    Lineage-specific rediploidization is a mechanism to explain time-lags between genome duplication and evolutionary diversification by Fiona M. Robertson, Manu Kumar Gundappa, Fabian Grammes, Torgeir R. Hvidsten, Anthony K. Redmond, Sigbjørn Lien, Samuel A. M. Martin, Peter W. H. Holland, Simen R. Sandve, Daniel J. Macqueen

    Published 2017-06-01
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    Article
  2. 2
    OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

    OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect by Kyle Thompson, Nicole Mai, Monika Oláhová, Filippo Scialó, Luke E Formosa, David A Stroud, Madeleine Garrett, Nichola Z Lax, Fiona M Robertson, Cristina Jou, Andres Nascimento, Carlos Ortez, Cecilia Jimenez‐Mallebrera, Steven A Hardy, Langping He, Garry K Brown, Paula Marttinen, Robert McFarland, Alberto Sanz, Brendan J Battersby, Penelope E Bonnen, Michael T Ryan, Zofia MA Chrzanowska‐Lightowlers, Robert N Lightowlers, Robert W Taylor

    Published 2018-11-01
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