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Molecular Vision|June 17, 2008
Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testingJohn Neidhardt, Esther Glaus, Birgit Lorenz, et al.
European Journal of Neurology|November 26, 2025
Tablet-Assisted Speech and Language Therapy for Acute Post-Stroke Aphasia: A Randomized Clinical Trial (LEXI Study)Johannes Wischmann, Leanna Brasch, Julia Franzen, et al.
Nature Communications|November 30, 2018
Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidisGuillaume Méric, Leonardos Mageiros, Johan Pensar, et al.
Blood|December 6, 2024
A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutationsNatalia Borbaran Bravo, Ekaterina Deordieva, Larissa Doll, et al.
Genome Research|April 11, 2014
Predicting the virulence of MRSA from its genome sequenceMaisem Laabei, Mario Recker, Justine K Rudkin, et al.
Auris, Nasus, Larynx|August 13, 2013
A multicenter observational study on the role of comorbidities in the recurrent episodes of benign paroxysmal positional vertigoAlessandro De Stefano, Francesco Dispenza, Hamlet Suarez, et al.
G3 (Bethesda, Md.)|October 13, 2017
Transcriptomic Analysis of Octanoic Acid Response in Drosophila sechellia Using RNA-SequencingStephen M Lanno, Sara M Gregory, Serena J Shimshak, et al.
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