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Human Molecular Genetics|April 12, 2017
Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesisCan Zhou, Chen Li, Bin Zhou, et al.American Journal of Medical Genetics. Part A|February 27, 2010
Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiencyCarolina Prando, Stéphanie Boisson-Dupuis, Audrey V Grant, et al.Human Molecular Genetics|September 1, 2007
Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrityQiuping Zhang, Cornelia Bethmann, Nathalie F Worth, et al.Pageof 26