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Deutsches Arzteblatt International|August 28, 2019
Hereditary Syndromes with Signs of Premature AgingDavor Lessel, Christian Kubisch
Current Opinion in Neurology|July 1, 2017
The rapid evolution of molecular genetic diagnostics in neuromuscular diseasesAlexander E Volk, Christian Kubisch
Biochemical and Biophysical Research Communications|June 6, 2016
Increased copper toxicity in Saccharomyces cerevisiae lacking VPS35, a component of the retromer and monogenic Parkinson disease gene in humansNadine Sowada, Barbara Stiller, Christian Kubisch
European Journal of Dermatology : EJD|March 23, 2012
Rare hereditary diseases with defects in DNA-repairJennifer Knoch, York Kamenisch, Christian Kubisch, et al.
Neurology|October 26, 2005
Early-onset toe walking in rippling muscle disease due to a new caveolin-3 gene mutationRicardo E Madrid, Christian Kubisch, Arthur P Hays
The Journal of Clinical Endocrinology and Metabolism|March 26, 2009
Genetic causes of goiter and deafness: Pendred syndrome in a girl and cooccurrence of Pendred syndrome and resistance to thyroid hormone in her sisterGuntram Borck, Ora Seewi, Alexander Jung, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
Arterial rupture in classic Ehlers-Danlos syndrome with COL5A1 mutationGuntram Borck, Peter Beighton, Christian Wilhelm, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 29, 2015
Serotonin reuptake inhibitors and serotonin transporter genotype modulate performance monitoring functions but not their electrophysiological correlatesAdrian G Fischer, Tanja Endrass, Martin Reuter, et al.
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