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Journal of Medical Genetics|May 3, 2005
Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathyT Rossenbacker, E Schollen, C Kuipéri, et al.
Human Molecular Genetics|July 7, 2001
Recombination hotspot in NF1 microdeletion patientsC López-Correa, M Dorschner, H Brems, et al.
Journal of Manipulative and Physiological Therapeutics|November 8, 2025
Effect of Cervical Lateral Flexion Prepositioning on Segmental Cervical Axial Rotation of C1 and C2: A Computed Tomography Cadaveric InvestigationAnja Matthijs, Omer C G Matthijs, Gunther Ch Windisch, et al.
PM & R : the Journal of Injury, Function, and Rehabilitation|September 18, 2013
Co-contractive activation of the superficial multifidus during volitional preemptive abdominal contractionOmer C G Matthijs, Gregory S Dedrick, C Roger James, et al.
Journal of Inherited Metabolic Disease|October 27, 2009
RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylationJ Jaeken, W Vleugels, L Régal, et al.
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