Showing results (311-320 of 338) with videos related to
Sort By:
Pageof 34
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 11, 2022
Muscle Strength and Physical Performance Are Associated With Risk of Postfracture Mortality But Not Subsequent Fracture in MenDima A Alajlouni, Dana Bliuc, Thach S Tran, et al.Nanoscale Research Letters|February 8, 2021
Structure Investigations of Islands with Atomic-Scale Boron-Carbon Bilayers in Heavily Boron-Doped Diamond Single Crystal: Origin of Stepwise Tensile StressS N Polyakov, V N Denisov, V V Denisov, et al.Optics Express|February 12, 2014
Hybrid diamond-silicon angular-dispersive x-ray monochromator with 0.25-meV energy bandwidth and high spectral efficiencyS Stoupin, Y V Shvyd'ko, D Shu, et al.Annals of the New York Academy of Sciences|January 22, 2009
Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humansPhilip F Giampietro, Sally L Dunwoodie, Kenro Kusumi, et al.Expert Opinion on Medical Diagnostics|March 19, 2013
Molecular diagnosis of vertebral segmentation disorders in humansPhilip F Giampietro, Sally L Dunwoodie, Kenro Kusumi, et al.JAMA Network Open|October 10, 2022
Association of Multimorbidity and Excess Mortality After Fractures Among Danish AdultsThach Tran, Dana Bliuc, Thao Ho-Le, et al.American Journal of Medical Genetics. Part A|October 17, 2006
DLL3 as a candidate gene for vertebral malformationsPhilip F Giampietro, Cathleen L Raggio, Cory Reynolds, et al.Scoliosis|September 25, 2007
Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformationsNader Ghebranious, Cathleen L Raggio, Robert D Blank, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 10, 2008
A missense T (Brachyury) mutation contributes to vertebral malformationsNader Ghebranious, Robert D Blank, Cathleen L Raggio, et al.American Journal of Medical Genetics. Part A|October 29, 2014
Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromesPhilip F Giampietro, Linlea Armstrong, Alex Stoddard, et al.Pageof 34