Domestic animal genetics.

por Tosso Leeb
Publicado 2021

A genome-wide association study to detect QTL for commercially important traits in Swiss Large White boars.

por Doreen Becker, Klaus Wimmers, Henning Luther, Andreas Hofer, Tosso Leeb
Publicado 2013

<i>LAMA2</i> Nonsense Variant in an Italian Greyhound with Congenital Muscular Dystrophy

por Matthias Christen, Victoria Indzhova, Ling T. Guo, Vidhya Jagannathan, Tosso Leeb, G. Diane Shelton, Josep Brocal
Publicado 2021

Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs.

por Matthias Christen, Sandra Högler, Miriam Kleiter, Michael Leschnik, Corinna Weber, Denise Thaller, Vidhya Jagannathan, Tosso Leeb
Publicado 2021

A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption).

por Marta Owczarek-Lipska, Vidhya Jagannathan, Cord Drögemüller, Sabina Lutz, Barbara Glanemann, Tosso Leeb, Peter H Kook
Publicado 2013

A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers.

por Theresa-Bernadette Mausberg, Gerhard Wess, Julia Simak, Lisa Keller, Michaela Drögemüller, Cord Drögemüller, Matthew T Webster, Hannah Stephenson, Joanna Dukes-McEwan, Tosso Leeb
Publicado 2011

A nonsense mutation in the IKBKG gene in mares with incontinentia pigmenti.

por Rachel E Towers, Leonardo Murgiano, David S Millar, Elise Glen, Ana Topf, Vidhya Jagannathan, Cord Drögemüller, Judith A Goodship, Angus J Clarke, Tosso Leeb
Publicado 2013

A hypomyelinating leukodystrophy in German Shepherd dogs

por Pia R. Quitt, Andreas Brühschwein, Kaspar Matiasek, Franziska Wielaender, Veera Karkamo, Marjo K. Hytönen, Andrea Meyer‐Lindenberg, Berett Dengler, Tosso Leeb, Hannes Lohi, Andrea Fischer
Publicado 2021

A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism.

por Mirjam Frischknecht, Helena Niehof-Oellers, Vidhya Jagannathan, Marta Owczarek-Lipska, Cord Drögemüller, Elisabeth Dietschi, Gaudenz Dolf, Bernd Tellhelm, Johann Lang, Katriina Tiira, Hannes Lohi, Tosso Leeb
Publicado 2013

An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle.

por Cord Drögemüller, Ursula Reichart, Torsten Seuberlich, Anna Oevermann, Martin Baumgartner, Kathrin Kühni Boghenbor, Michael H Stoffel, Claudia Syring, Mireille Meylan, Simone Müller, Mathias Müller, Birgit Gredler, Johann Sölkner, Tosso Leeb
Publicado 2011