يعرض 11 - 20 نتائج من 500 نتيجة بحث عن '"Mautner, Victor-Felix"', وقت الاستعلام: 1.00s تنقيح النتائج
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    المؤلفون: Özden, Cansu1 (AUTHOR) c.oezden@uke.de, Mautner, VictorFelix2 (AUTHOR), Farschtschi, Said2 (AUTHOR), Molwitz, Isabel1 (AUTHOR), Ristow, Inka1 (AUTHOR), Bannas, Peter1 (AUTHOR), Well, Lennart1 (AUTHOR), Klutmann, Susanne1 (AUTHOR), Adam, Gerhard1 (AUTHOR), Apostolova, Ivayla1 (AUTHOR), Buchert, Ralph1 (AUTHOR)

    المصدر: Journal of Neuroimaging. Jan/Feb2024, Vol. 34 Issue 1, p138-144. 7p.

  2. 12
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    وصف الملف: application/pdf

    العلاقة: https://orca.cardiff.ac.uk/id/eprint/146891/7/genes-12-01639-v3.pdfTest; Kehrer-Sawatzki, Hildegard, Wahlländer, Ute, Cooper, David N. https://orca.cardiff.ac.uk/view/cardiffauthors/A0547623.htmlTest orcid:0000-0002-8943-8484 orcid:0000-0002-8943-8484 and Mautner, Victor-Felix 2021. Atypical NF1 microdeletions: challenges and opportunities for Genotype/Phenotype correlations in patients with large NF1 deletions. Genes 12 (10) , 1639. 10.3390/genes12101639 https://doi.org/10.3390/genes12101639Test file https://orca.cardiff.ac.uk/id/eprint/146891/7/genes-12-01639-v3.pdfTest

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    المؤلفون: Koelsche, Christian, Schrimpf, Daniel, Stichel, Damian, Sill, Martin, Sahm, Felix, Reuss, David E., Blattner, Mirjam, Worst, Barbara, Heilig, Christoph E., Beck, Katja, Horak, Peter, Mautner, Victor-Felix, Schittenhelm, Jens, Serrano, Jonathan, Snuderl, Matija, Büttner, Reinhard, Klingebiel, Thomas, Buslei, Rolf, Gessler, Manfred, Wesseling, Pieter, Brandner, Sebastian, Jaunmuktane, Zane, Dinjens, Winand N. M., Lyskjær, Iben, Schirmacher, Peter, Stenzinger, Albrecht, Brors, Benedikt, Glimm, Hanno, Heining, Christoph, Tirado, Oscar M., Sáinz Jaspeado, Miguel Guillermo, Alonso, Javier, García del Muro Solans, Xavier, Mora Salvador, Jaume, Moran, Sebastian, Esteller, Manel, Benhamida, Jamal K., Ladanyi, Marc, Wardelmann, Eva, Antonescu, Cristina, Flanagan, Adrienne, Dirksen, Uta, Baumhoer, Daniel, Hartmann, Wolfgang, Hohenberger, Peter, Vokuhl, Christian, Flucke, Uta, Petersen, Iver, Mechtersheimer, Gunhild, Capper, David, Jones, David T. W., Fröhling, Stefan, Pfister, Stefan M., Kreutzfeldt, Simon, Paff, Elke, von Deimling, Andreas, Stark, Sebastian, Johann, Pascal, Selt, Florian, Ecker, Jonas, Sturm, Dominik, Pajtler, Kristian W., Reinhardt, Annekathrin, Wefers, Annika K., Sievers, Philipp, Suwala, Abigail, Ebrahimi, Azadeh, Fernández Klett, Francisco, Casalini, Belén, Korshunov, Andrey, Hovestadt, Volker, Kommoss, Felix K. F., Kriegsmann, Mark, Schick, Matthias, Bewerunge-Hudler, Melanie, Milde, Till, Kulozik, Andreas E., Witt, Olaf, Kool, Marcel, Romero-pérez, Laura, Grünewald, Thomas G. P., Kirchner, Thomas, Wick, Wolfgang, Platten, Michael, Unterberg, Andreas, Uhl, Matthias, Abdollahi, Amir, Lehner, Burkhard, Debus, Jürgen, Thomas, Christian, Hasselblatt, Martin, Paulus, Werner, Hartmann, Christian, Staszewski, Ori, Prinz, Marco, Hench, Jürgen, Frank, Stephan, Versleijen-Jonkers, Yvonne M. H., Mentzel, Thomas, Weidema, Marije E., Griewank, Klaus, Álava, Enrique de, Martín, Juan Díaz, Idoate Gastearena, Miguel A., Chang, Kenneth Tou-En, Low, Sharon Yin Yee, Cuevas-Bourdier, Adrian, Mittelbronn, Michel, Mynarek, Martin, Schüller, Ulrich, Rutkowski, Stefan

    المصدر: Articles publicats en revistes (Ciències Fisiològiques)

    مصطلحات موضوعية: Sarcoma, ADN, DNA

    وصف الملف: 10 p.; application/pdf

    العلاقة: Reproducció del document publicat a: https://doi.org/10.1038/s41467-020-20603-4Test; Nature Communications, 2021, vol. 12; https://doi.org/10.1038/s41467-020-20603-4Test; http://hdl.handle.net/2445/174293Test; 716103

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    المساهمون: bundesverband neurofibromatose organization

    المصدر: Orphanet Journal of Rare Diseases ; volume 16, issue 1 ; ISSN 1750-1172