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  2. Daniels, Dieter [Editor]; Schmidt, Barbara U. [Editor] ; Ludwig-Boltzmann-Institut Medien, Kunst, Forschung Linz

    Artists as inventors - inventors as artists

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    Ostfildern: Hatje Cantz, 2008

  3. Borck, Karin [Other]; Janus, Eligiusz [Other]; Madajczyk, Czesław [Other]; Meissner, Blanka [Other]; Hahn, Hans Henning [Other]; Müller, Michael [Other]; Biernacki, Stanisław [Other]

    Vom Generalplan Ost zum Generalsiedlungsplan : Dokumente

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    Berlin: De Gruyter, 2011

    Published in: Einzelveröffentlichungen der Historischen Kommission zu Berlin ; 80

  6. Marroquin, Nicolai; Stranz, Sebastian; Müller, Kathrin; Wieland, Thomas; Ruf, Wolfgang P.; Brockmann, Sarah J.; Danzer, Karin M.; Borck, Guntram; Hübers, Annemarie; Weydt, Patrick; Meitinger, Thomas; Strom, Tim-Matthias; Rosenbohm, Angela; Ludolph, Albert C.; Weishaupt, Jochen H.

    Screening forCHCHD10mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant: Table 1

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    Oxford University Press (OUP), 2016

    Published in: Brain

  7. Brenner, David; Müller, Kathrin; Wieland, Thomas; Weydt, Patrick; Böhm, Sarah; Lulé, Dorothée; Hübers, Annemarie; Neuwirth, Christoph; Weber, Markus; Borck, Guntram; Wahlqvist, Magnus; Danzer, Karin M.; Volk, Alexander E.; Meitinger, Thomas; Strom, Tim M.; Otto, Markus; Kassubek, Jan; Ludolph, Albert C.; Andersen, Peter M.; Weishaupt, Jochen H.

    NEK1mutations in familial amyotrophic lateral sclerosis

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    Oxford University Press (OUP), 2016

    Published in: Brain

  8. Kast, Karin; Rhiem, Kerstin; Wappenschmidt, Barbara; Hahnen, Eric; Hauke, Jan; Bluemcke, Britta; Zarghooni, Verena; Herold, Natalie; Ditsch, Nina; Kiechle, Marion; Braun, Michael; Fischer, Christine; Dikow, Nicola; Schott, Sarah; Rahner, Nils; Niederacher, Dieter; Fehm, Tanja; Gehrig, Andrea; Mueller-Reible, Clemens; Arnold, Norbert; Maass, Nicolai; Borck, Guntram; de Gregorio, Nikolaus; Scholz, Caroline; [...]

    Prevalence ofBRCA1/2germline mutations in 21 401 families with breast and ovarian cancer

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    BMJ, 2016

    Published in: Journal of Medical Genetics

  9. Basel-Vanagaite, Lina; Dallapiccola, Bruno; Ramirez-Solis, Ramiro; Segref, Alexandra; Thiele, Holger; Edwards, Andrew; Arends, Mark J.; Miró, Xavier; White, Jacqueline K.; Désir, Julie; Abramowicz, Marc; Dentici, Maria Lisa; Lepri, Francesca; Hofmann, Kay; Har-Zahav, Adi; Ryder, Edward; Karp, Natasha A.; Estabel, Jeanne; Gerdin, Anna-Karin B.; Podrini, Christine; Ingham, Neil J.; Altmüller, Janine; Nürnberg, Gudrun; Frommolt, Peter; [...]

    Deficiency for the Ubiquitin Ligase UBE3B in a Blepharophimosis-Ptosis-Intellectual-Disability Syndrome

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    Elsevier BV, 2012

    Published in: The American Journal of Human Genetics

  10. Brenner, David; Rosenbohm, Angela; Yilmaz, Rüstem; Müller, Kathrin; Grehl, Torsten; Petri, Susanne; Meyer, Thomas; Grosskreutz, Julian; Weydt, Patrick; Ruf, Wolfgang; Neuwirth, Christoph; Weber, Markus; Pinto, Susana; Claeys, Kristl G; Schrank, Berthold; Jordan, Berit; Knehr, Antje; Günther, Kornelia; Hübers, Annemarie; Zeller, Daniel; Kubisch, Christian; Jablonka, Sibylle; Sendtner, Michael; Klopstock, Thomas; [...]

    Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations

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    Oxford University Press (OUP), 2019

    Published in: Brain

  11. Brenner, David; Yilmaz, Rüstem; Müller, Kathrin; Grehl, Torsten; Petri, Susanne; Meyer, Thomas; Grosskreutz, Julian; Weydt, Patrick; Ruf, Wolfgang; Neuwirth, Christoph; Weber, Markus; Pinto, Susana; Claeys, Kristl G; Schrank, Berthold; Jordan, Berit; Knehr, Antje; Günther, Kornelia; Hübers, Annemarie; Zeller, Daniel; Kubisch, Christian; Jablonka, Sibylle; Sendtner, Michael; Klopstock, Thomas; de Carvalho, Mamede; [...]

    Hot-spot KIF5A mutations cause familial ALS

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    Oxford University Press (OUP), 2018

    Published in: Brain