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Journal of the American Society of Nephrology : JASN|July 26, 2002
Linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1John J Neary, Peter J Conlon, David Croke, et al.Human Molecular Genetics|May 23, 1998
Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathyT C Pan, R Z Zhang, M A Pericak-Vance, et al.Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
AD plasma biomarkers are stable for an extended period at -20°C: implications for resource-constrained environmentsBiniyam A Ayele, Patrice L Whitehead, Julianna Pascual, et al.Physical Therapy|July 19, 2026
Perspectives of Private Practice Physical Therapy Health Care Systems Participating in a Pragmatic Clinical Trial: A Qualitative StudyBarbara J Van Gorp, Elizabeth Johnson, Kari Vance, et al.Journal of the American Heart Association|October 4, 2016
Novel Role for Matrix Metalloproteinase 9 in Modulation of Cholesterol MetabolismSamuel Hernandez-Anzaldo, Vesna Brglez, Bianca Hemmeryckx, et al.American Journal of Human Genetics|February 15, 2001
A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosisR R Allingham, B Seo, E Rampersaud, et al.Human Genetics|April 14, 2005
Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson diseaseMaher A Noureddine, Xue-Jun Qin, Sofia A Oliveira, et al.Experimental Neurology|May 1, 1989
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17J M Vance, G A Nicholson, L H Yamaoka, et al.Pain Medicine (Malden, Mass.)|March 20, 2014
A practice audit of CT-guided injections of pars interarticularis defects in patients with axial low back pain: a primer for further investigationJohn T Wald, Jennifer R Geske, Felix E Diehn, et al.Annals of Neurology|November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13J M Stajich, J M Gilchrist, F Lennon, et al.Pageof 645