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Nature Genetics|May 1, 2012
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndromeDavid A Koolen, Jamie M Kramer, Kornelia Neveling, et al.
Journal of the American College of Cardiology|January 8, 2025
Demographic-Based Personalized Left Ventricular Hypertrophy Thresholds for Hypertrophic Cardiomyopathy DiagnosisHunain Shiwani, Rhodri H Davies, Constantin-Cristian Topriceanu, et al.
Monthly Notices of the Royal Astronomical Society|June 10, 2016
New methods to constrain the radio transient rate: results from a survey of four fields with LOFARD Carbone, A J van der Horst, R A M J Wijers, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|April 8, 2018
Reproducibility and Repeatability of Semiquantitative <sup>18</sup>F-Fluorodihydrotestosterone Uptake Metrics in Castration-Resistant Prostate Cancer Metastases: A Prospective Multicenter StudyHebert Alberto Vargas, Gem M Kramer, Andrew M Scott, et al.
Physical Review Letters|August 12, 2025
First Search for Axion Dark Matter with a MADMAX PrototypeB Ary Dos Santos Garcia, D Bergermann, A Caldwell, et al.
Physical Review Letters|August 8, 2015
Limits on Anisotropy in the Nanohertz Stochastic Gravitational Wave BackgroundS R Taylor, C M F Mingarelli, J R Gair, et al.
JACC. Clinical Electrophysiology|July 4, 2021
Predictors of Major Atrial Fibrillation Endpoints in the National Heart, Lung, and Blood Institute HCMRChristopher M Kramer, John P DiMarco, Paul Kolm, et al.
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