Search Results - Admard, Jakob

Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients by Menzel, Michael (Author) , Ossowski, Stephan (Author) , Kral, Sebastian (Author) , Metzger, Patrick (Author) , Horak, Peter (Author) , Marienfeld, Ralf (Author) , Börries, Melanie (Author) , Wolter, Steffen (Author) , Ball, Markus (Author) , Neumann, Olaf (Author) , Armeanu-Ebinger, Sorin (Author) , Schroeder, Christopher (Author) , Matysiak, Uta (Author) , Goldschmid, Hannah (Author) , Schipperges, Vincent (Author) , Fürstberger, Axel (Author) , Allgäuer, Michael (Author) , Eberhardt, Timo (Author) , Niewöhner, Jakob (Author) , Blaumeiser, Andreas (Author) , Plöger, Carolin (Author) , Haack, Tobias (Author) , Tay, Timothy Kwang Yong (Author) , Kelemen, Olga (Author) , Pauli, Thomas Dieter (Author) , Kirchner, Martina (Author) , Kluck, Klaus (Author) , Ott, Alexander (Author) , Renner, Marcus (Author) , Admard, Jakob (Author) , Gschwind, Axel (Author) , Laßmann, Silke (Author) , Kestler, Hans A. (Author) , Fend, Falko (Author) , Illert, Anna Lena (Author) , Werner, Martin (Author) , Möller, Peter (Author) , Seufferlein, Thomas Theodor Werner (Author) , Malek, Nisar Peter (Author) , Schirmacher, Peter (Author) , Fröhling, Stefan (Author) , Kazdal, Daniel (Author) , Budczies, Jan (Author) , Stenzinger, Albrecht (Author) ,

• kostenfrei
• kostenfrei

Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy by Park, Joohyun (Author) , Tucci, Arianna (Author) , Cipriani, Valentina (Author) , Demidov, German (Author) , Rocca, Clarissa (Author) , Senderek, Jan (Author) , Butryn, Michaela (Author) , Velic, Ana (Author) , Lam, Tanya (Author) , Galanaki, Evangelia (Author) , Cali, Elisa (Author) , Vestito, Letizia (Author) , Maroofian, Reza (Author) , Deininger, Natalie (Author) , Rautenberg, Maren (Author) , Admard, Jakob (Author) , Hahn, Gesa-Astrid (Author) , Bartels, Claudius (Author) , Os, Nienke J. H. van (Author) , Horvath, Rita (Author) , Chinnery, Patrick F. (Author) , Tiet, May Yung (Author) , Hewamadduma, Channa (Author) , Hadjivassiliou, Marios (Author) , Tofaris, George K. (Author) , Wood, Nicholas (Author) , Hayer, Stefanie Nicole (Author) , Bender, Friedemann (Author) , Menden, Benita (Author) , Cordts, Isabell (Author) , Klein, Katrin (Author) , Nguyen, Huu Phuc (Author) , Krauss, Joachim K. (Author) , Blahak, Christian (Author) , Strom, Tim M. (Author) , Sturm, Marc (Author) , Warrenburg, Bart Petrus Christoffel van de (Author) , Lerche, Holger (Author) , Maček, Boris (Author) , Synofzik, Matthis (Author) , Ossowski, Stephan (Author) , Timmann-Braun, Dagmar (Author) , Wolf, Marc (Author) , Smedley, Damian (Author) , Rieß, Olaf (Author) , Schöls, Ludger (Author) , Houlden, Henry (Author) , Haack, Tobias (Author) , Hengel, Holger (Author) ,

• lizenzpflichtig
• lizenzpflichtig

Bi-allelic truncating mutations in VWA1 cause neuromyopathy by Deschauer, Marcus (Author) , Hengel, Holger (Author) , Rupprich, Katrin (Author) , Kreiß, Martina (Author) , Schlotter-Weigel, Beate (Author) , Grimmel, Mona (Author) , Admard, Jakob (Author) , Schneider, Ilka (Author) , Alhaddad, Bader (Author) , Gazou, Anastasia (Author) , Sturm, Marc (Author) , Vorgerd, Matthias (Author) , Balousha, Ghassan (Author) , Balousha, Osama (Author) , Falna, Mohammed (Author) , Kirschke, Jan S. (Author) , Kornblum, Cornelia (Author) , Jordan, Berit (Author) , Kraya, Torsten (Author) , Strom, Tim M. (Author) , Weis, Joachim (Author) , Schöls, Ludger (Author) , Schara, Ulrike (Author) , Zierz, Stephan (Author) , Riess, Olaf (Author) , Meitinger, Thomas (Author) , Haack, Tobias B. (Author) ,

• lizenzpflichtig