Identification of 34 novel and 56 known<i>FOXL2</i>mutations in patients with blepharophimosis syndrome
Diane Beysen(Antwerp University Hospital), Paul Laissue(Inserm), Patricia Delbeke(Ghent University Hospital), Bart P. Leroy(Ghent University Hospital), Dalit Barel(Tel Aviv Sourasky Medical Center), Friedrich Ebinger(Defence Research and Development Organisation), Rachel Laframboise, Nicole Van Regemorter(Centre Hospitalier Universitaire Brugmann), Reiner A. Veitia(Centre National de la Recherche Scientifique), David Mowat(UNSW Sydney), Regina Ensenauer(Zimmer Biomet (Netherlands)), Philippe Touraine(Sorbonne Université), Raoul C. M. Hennekam(University of Amsterdam), Virginia Kimonis(University of California, Irvine), Jill Clayton‐Smith(St Mary's Hospital), Thomy de Ravel(KU Leuven), Sarah De Jaegere(Ghent University Hospital), Dagmar Wieczorek(Essen University Hospital), David J. Amor(The University of Melbourne), Nina Øyen(Haukeland University Hospital), David T. Miller(Boston Children's Hospital), Astrid S. Plomp, Yvonne Hendriks(Amsterdam UMC Location University of Amsterdam), Philippe Bouchard(Sorbonne Université), Louise C. Wilson(Great Ormond Street Hospital for Children NHS Foundation Trust), Anne De Paepe(Ghent University Hospital), Marc Fellous(Inserm), Christian Decock(Ghent University Hospital), Sophie Christin-Maître(Inserm), Françoise Meire(Ghent University Hospital), Luitgard M. Neumann(Praxis für Humangenetik), Gabriele Gillessen‐Kaesbach(University Hospital Schleswig-Holstein), Kathleen A. Leppig(Group Health Cooperative), Arthur W. Grix(Kaiser Permanente)
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