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European Journal of Human Genetics : EJHG|June 5, 2008
Novel homozygous ALS2 nonsense mutation (p.Gln715X) in sibs with infantile-onset ascending spastic paralysis: the first cases from northwestern EuropeCorien C Verschuuren-Bemelmans, Pia Winter, Deborah A Sival, et al.
American Journal of Medical Genetics. Part A|March 19, 2008
Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophyBirgit Zirn, Wolfram Kress, Tiemo Grimm, et al.
Bjpsych Bulletin|December 7, 2023
UK adult ADHD services in crisisMichael C F Smith, Raja A S Mukherjee, Ulrich Müller-Sedgwick, et al.
American Journal of Human Genetics|February 12, 2004
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous familyStephan Niemann, Chengfeng Zhao, Filon Pascu, et al.
The Journal of Cell Biology|September 17, 2008
Laminins promote postsynaptic maturation by an autocrine mechanism at the neuromuscular junctionHiroshi Nishimune, Gregorio Valdez, George Jarad, et al.
The European Journal of Neuroscience|January 28, 2014
Thrombospondins 1 and 2 are important for afferent synapse formation and function in the inner earDiana Mendus, Srividya Sundaresan, Nicolas Grillet, et al.
F1000Research|April 10, 2020
Preconditioning strategies to prevent acute kidney injuryMartin Richard Späth, Felix Carlo Koehler, Karla Johanna Ruth Hoyer-Allo, et al.
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