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Human Mutation|October 26, 2017
Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathiesWenjuan Zhang, S Paige Taylor, Hayley A Ennis, et al.Health Promotion Practice|April 26, 2006
Collaborative design and implementation of a multisite community coalition evaluationLaurie L Lachance, Christy R Houle, Elaine F Cassidy, et al.Perfusion|February 23, 2007
Early results of a comprehensive operative and perfusion strategy to attenuate the incidence of adverse neurological outcomes in on-pump coronary artery bypass grafting (CABG) patientsKevin J Lilly, Jorge M Balaguer, Paul A Pirundini, et al.American Journal of Human Genetics|July 27, 1999
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase geneA Colige, A L Sieron, S W Li, et al.Annals of Surgical Oncology|November 11, 2006
Lymphatic drainage of the peritoneal space: a pattern dependent on bowel lymphaticsCherie P Parungo, David I Soybel, Yolonda L Colson, et al.Ebiomedicine|November 26, 2020
Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasiaMaya Barad, Fabiana Csukasi, Michaela Bosakova, et al.Nature Biotechnology|December 9, 2003
Near-infrared fluorescent type II quantum dots for sentinel lymph node mappingSungjee Kim, Yong Taik Lim, Edward G Soltesz, et al.American Journal of Human Genetics|November 2, 2010
Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen geneStuart W Tompson, Carlos A Bacino, Nicole P Safina, et al.The Journal of Thoracic and Cardiovascular Surgery|March 4, 2016
Are homografts superior to conventional prosthetic valves in the setting of infective endocarditis involving the aortic valve?Joon Bum Kim, Julius I Ejiofor, Maroun Yammine, et al.Plos One|May 21, 2010
Generalized connective tissue disease in Crtap-/- mouseDustin Baldridge, Jennifer Lennington, MaryAnn Weis, et al.Pageof 72