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Human Mutation|January 27, 2021
Severe congenital lactic acidosis and hypertrophic cardiomyopathy caused by an intronic variant in NDUFB7Sandrina P Correia, Marco F Moedas, Karin Naess, et al.
Journal of Medical Genetics|June 19, 2015
Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acidChristoph Freyer, Henrik Stranneheim, Karin Naess, et al.
Urologia Internationalis|August 30, 2014
The clinical use of statistical permutation test methodology: a tool for identifying predictive variables of outcomeM Racioppi, L Salmaso, C Brombin, et al.
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