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American Journal of Human Genetics|June 19, 2026
De novo variants in LDB1 are linked to distinct neurodevelopmental phenotypes determined by variant location and differing pathomechanismsRebecca Fluri, Mireia Coll-Tané, Theresa Brunet, et al.
Frontiers in Neurology|July 30, 2026
Real-world practices and challenges of radiologically isolated syndrome: results of a cross-sector survey by the DACH MS guidelines groupFriederike Held, Antonios Bayas, Katharina Christe, et al.
Molecular Psychiatry|January 6, 2018
Genetics of intellectual disability in consanguineous familiesHao Hu, Kimia Kahrizi, Luciana Musante, et al.
Neurology|November 11, 2018
Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of diseaseSara Zagaglia, Christina Selch, Jelena Radic Nisevic, et al.
Nature Immunology|March 26, 2026
A transcriptomic microglia taxonomy across mouse and human pathologiesChintan Chhatbar, Roman Sankowski, Michael Schulz, et al.
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