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Neuroepidemiology|May 16, 2022
Genetic Epidemiology of Amyotrophic Lateral Sclerosis in Norway: A 2-Year Population-Based StudyCathrine Goberg Olsen, Øyvind Løvold Busk, Tori Navestad Aanjesen, et al.Physical Review Letters|June 6, 2017
Gamma Decay of Unbound Neutron-Hole States in ^{133}SnV Vaquero, A Jungclaus, P Doornenbal, et al.American Journal of Human Genetics|October 12, 2023
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomaliesZelha Nil, Ashish R Deshwar, Yan Huang, et al.Physical Review Letters|September 4, 2008
0(gs)+ -->2(1)+ transition strengths in 106Sn and 108SnA Ekström, J Cederkäll, C Fahlander, et al.American Journal of Medical Genetics. Part A|September 13, 2021
Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobinCharlotte von der Lippe, Kristian Tveten, Trine E Prescott, et al.American Journal of Human Genetics|October 29, 2024
Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemiaScott Barish, Sheng-Jia Lin, Reza Maroofian, et al.Science Advances|February 17, 2023
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sitesNicola de Prisco, Caitlin Ford, Nathan D Elrod, et al.European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathiesBo Yuan, Juanita Neira, Davut Pehlivan, et al.Physical Review Letters|June 17, 2017
Anomalies in the Charge Yields of Fission Fragments from the ^{238}U(n,f) ReactionJ N Wilson, M Lebois, L Qi, et al.Pageof 18