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Neurogenetics|March 22, 2012
Frequency of SMARCB1 mutations in familial and sporadic schwannomatosisMiriam J Smith, Andrew J Wallace, Naomi L Bowers, et al.
International Journal of Speech-Language Pathology|October 30, 2012
The World Report on Disability as a blueprint for international, national, and local aphasia servicesLinda E Worrall, Tami Howe, Anna O'Callaghan, et al.
Scientific Reports|January 19, 2025
Alterations in genes associated with cytosolic RNA sensing in whole blood are associated with coronary microvascular disease in SLELihong Huo, Arati Naveen Kumar, Gantsetseg Tumurkhuu, et al.
European Journal of Human Genetics : EJHG|June 9, 2016
Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testingHelen Byers, Yvonne Wallis, Elke M van Veen, et al.
Journal of Synchrotron Radiation|July 31, 2025
3DMPR - a robust morphological approach for applying phase retrieval in proximity to highly attenuating objects in computed tomographyJames A Pollock, L C P Croton, K S Morgan, et al.
Disability and Rehabilitation|June 9, 2025
International priorities for a unified aphasia awareness campaign: a nominal group technique study across five countriesClaire Bennington, Jytte Isaksen, Ciara Shiggins, et al.
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