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Physical Review Letters|November 24, 2018
Pseudospin Symmetry and Microscopic Origin of Shape Coexistence in the ^{78}Ni Region: A Hint from Lifetime MeasurementsC Delafosse, D Verney, P Marević, et al.
Sleep & Breathing = Schlaf & Atmung|December 24, 2018
Sex differences in mandibular repositioning device therapy effectiveness in patients with obstructive sleep apnea syndromeMarie-Françoise Vecchierini, Valérie Attali, Jean-Marc Collet, et al.
Journal of Personalized Medicine|September 23, 2022
Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled AnalysisSandrine Morel, Isabel C Hostettler, Georg R Spinner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 9, 2022
Rare pathogenic variants in WNK3 cause X-linked intellectual disabilitySébastien Küry, Jinwei Zhang, Thomas Besnard, et al.
Physical Review Letters|November 5, 2023
Measurement of the 2νββ Decay Rate and Spectral Shape of ^{100}Mo from the CUPID-Mo ExperimentC Augier, A S Barabash, F Bellini, et al.
Nature Genetics|November 17, 2020
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factorsMark K Bakker, Rick A A van der Spek, Wouter van Rheenen, et al.
Physical Review Letters|May 21, 2021
New Limit for Neutrinoless Double-Beta Decay of ^{100}Mo from the CUPID-Mo ExperimentE Armengaud, C Augier, A S Barabash, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 4, 2021
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behaviorHolly K Harris, Tojo Nakayama, Jenny Lai, et al.
American Journal of Human Genetics|December 31, 2022
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotypeSusan M Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano, et al.
Brain : a Journal of Neurology|December 1, 2023
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypesBerardo Rinaldi, Allan Bayat, Linda G Zachariassen, et al.
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