Showing 1 - 2 results of 2 for search 'Elisabet Einarsdottir', query time: 0.01s Refine Results
  1. 1
    Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report

    Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report by 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

    Published 2020
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  2. 2
    Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma

    Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma by 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

    Published 2020
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