Torthaí cuardaigh - Elisabet Einarsdottir

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  1. 1
    Íomhá chlúdaigh

    Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report de réir Andrea Bieder, Elisabet Einarsdottir, Hans Matsson, Harriet E. Nilsson, Jesper Eisfeldt, Anca Dragomir, Martin Paucar, Tobias Granberg, Tie-Qiang Li, Anna Lindstrand, Juha Kere, Isabel Tapia-Páez

    Foilsithe / Cruthaithe 2020
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  2. 2
    Íomhá chlúdaigh

    Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma de réir Liisa Harjama, Kaisa Kettunen, Outi Elomaa, Elisabet Einarsdottir, Hannele Heikkilä, Sirpa Kivirikko, Katriina Lappalainen, Janna Saarela, Caroline Alby, Annamari Ranki, Juha Kere, Smail Hadj-Rabia, Katariina Hannula-Jouppi

    Foilsithe / Cruthaithe 2020
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