Search Results - Tinschert, Sigrid

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    Phacomatosis pigmentokeratotica is caused by a postzygotic HRAS mutation in a multipotent progenitor cell by Größer, Leopold (Author) , Herschberger, Eva (Author) , Sagrera, Ana (Author) , Shwayder, Tor (Author) , Flux, Katharina (Author) , Ehmann, Laura (Author) , Wollenberg, Andreas (Author) , Torrelo, Antonio (Author) , Bagazgoitia, Lorea (Author) , Diaz-Ley, Blanca (Author) , Tinschert, Sigrid (Author) , Oschlies, Ilske (Author) , Singer, Sebastian (Author) , Mickler, Marion (Author) , Toll, Agusti (Author) , Landthaler, Michael (Author) , Real, Francisco X. (Author) , Hafner, Christian (Author) ,


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    Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia by Endris, Volker (Author) , Hackmann, Karl (Author) , Neuhann, Teresa M. (Author) , Grasshoff, Ute (Author) , Bonin, Michael (Author) , Haug, Ulrich (Author) , Hahn, Gabriele (Author) , Schallner, Jens C. (Author) , Schröck, Evelin (Author) , Tinschert, Sigrid (Author) , Rappold, Gudrun (Author) , Moog, Ute (Author) ,


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    Zunich neuroectodermal syndrome: migratory ichthyosiform dermatosis, colobomas, and other abnormalities by Tinschert, Sigrid (Author) , Anton-Lamprecht, Ingrun (Author) , Albrecht-Nebe, Helga (Author) , Audring, Heike (Author) ,


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