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The Medaka Inbred Kiyosu-Karlsruhe (MIKK) panel by Fitzgerald, Tomas (Author) , Brettell, Ian (Author) , Leger, Adrien (Author) , Wolf, Nadeshda (Author) , Kusminski, Natalja (Author) , Monahan, Jack (Author) , Barton, Carl (Author) , Herder, Cathrin (Author) , Aadepu, Narendar (Author) , Gierten, Jakob (Author) , Becker, Clara (Author) , Hammouda, Omar (Author) , Hasel, Eva Mareike (Author) , Lischik, Colin Q. (Author) , Lust, Katharina (Author) , Sokolova, Natalia (Author) , Suzuki, Risa (Author) , Tsingos, Erika (Author) , Tavhelidse-Suck, Tinatini (Author) , Thumberger, Thomas (Author) , Watson, Philip (Author) , Welz, Bettina (Author) , Khouja, Nadia (Author) , Naruse, Kiyoshi (Author) , Birney, Ewan (Author) , Wittbrodt, Joachim (Author) , Loosli, Felix (Author) ,

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The copy number variation and stroke (CaNVAS) risk and outcome study by Cole, John W. (Author) , Adigun, Taiwo (Author) , Akinyemi, Rufus (Author) , Akpa, Onoja Matthew (Author) , Bell, Steven (Author) , Chen, Bowang (Author) , Conde, Jordi Jimenez (Author) , Dobao, Uxue Lazcano (Author) , Fernandez, Israel (Author) , Fornage, Myriam (Author) , Gallego-Fabrega, Cristina (Author) , Jern, Christina (Author) , Krawczak, Michael (Author) , Lindgren, Arne (Author) , Markus, Hugh S. (Author) , Melander, Olle (Author) , Owolabi, Mayowa (Author) , Schlicht, Kristina (Author) , Söderholm, Martin (Author) , Srinivasasainagendra, Vinodh (Author) , Tárraga, Carolina Soriano (Author) , Stenman, Martin (Author) , Tiwari, Hemant (Author) , Corasaniti, Margaret (Author) , Fecteau, Natalie (Author) , Guizzardi, Beth (Author) , Lopez, Haley (Author) , Nguyen, Kevin (Author) , Gaynor, Brady (Author) , O’Connor, Timothy (Author) , Stine, O. Colin (Author) , Kittner, Steven J. (Author) , McArdle, Patrick (Author) , Mitchell, Braxton D. (Author) , Xu, Huichun (Author) , Grond-Ginsbach, Caspar (Author) ,

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Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay by Kobow, Katja (Author) , Jabari, Samir (Author) , Pieper, Tom (Author) , Kudernatsch, Manfred (Author) , Polster, Tilman (Author) , Woermann, Friedrich G. (Author) , Kalbhenn, Thilo (Author) , Hamer, Hajo (Author) , Rössler, Karl (Author) , Mühlebner, Angelika (Author) , Spliet, Wim G. M. (Author) , Feucht, Martha (Author) , Hou, Yanghao (Author) , Stichel, Damian (Author) , Korshunov, Andrey (Author) , Sahm, Felix (Author) , Coras, Roland (Author) , Blümcke, Ingmar (Author) , Deimling, Andreas von (Author) ,

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Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read... by Neuhaus, Christine (Author) , Rohrschneider, Klaus (Author) ,

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