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Human Mutation|April 26, 2019
Mutation update for the SATB2 geneYuri A Zarate, Katherine A Bosanko, Aisling R Caffrey, et al.Physical Review Letters|April 6, 2001
Measurement of the charged pion electromagnetic form factorJ Volmer, D Abbott, H Anklin, et al.Physical Review Letters|May 16, 2007
Longitudinal-transverse separations of deep-inelastic structure functions at low Q2 for hydrogen and deuteriumV Tvaskis, M E Christy, J Arrington, et al.Physical Review Letters|December 13, 2006
Determination of the pion charge form factor at Q2=1.60 and 2.45 (GeV/c)2T Horn, K Aniol, J Arrington, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2022
Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndromeJet van der Spek, Joery den Hoed, Lot Snijders Blok, et al.Neuron|March 6, 2020
Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical DevelopmentAshley L Lennox, Mariah L Hoye, Ruiji Jiang, et al.Nature Biotechnology|July 29, 2008
Genome sequence of the metazoan plant-parasitic nematode Meloidogyne incognitaPierre Abad, Jérôme Gouzy, Jean-Marc Aury, et al.Journal of Medical Genetics|August 4, 2025
Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with NF1 point variantsLaurence Pacot, Marinus Blok, Dominique Vidaud, et al.The World Allergy Organization Journal|September 19, 2022
Managing food allergy: GA2LEN guideline 2022Antonella Muraro, Debra de Silva, Susanne Halken, et al.Physical Review Letters|November 26, 2019
Unique Access to u-Channel Physics: Exclusive Backward-Angle Omega Meson ElectroproductionW B Li, G M Huber, H P Blok, et al.Pageof 159