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Neurology|April 14, 2004
LGI1 mutations in autosomal dominant partial epilepsy with auditory featuresR Ottman, M R Winawer, S Kalachikov, et al.Annals of Neurology|July 1, 1997
Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologuesC H Wang, T A Carter, K Das, et al.Progress in Retinal and Eye Research|June 30, 2016
Structural and molecular bases of rod photoreceptor morphogenesis and diseaseTheodore G Wensel, Zhixian Zhang, Ivan A Anastassov, et al.Journal of Geophysical Research. Atmospheres : JGR|June 14, 2021
Establishing the Suitability of the Model for Prediction Across Scales for Global Retrospective Air Quality ModelingRobert C Gilliam, Jerold A Herwehe, O Russell Bullock, et al.Neurology|April 1, 1995
Autosomal dominant distal spinal muscular atrophy in four generationsK B Boylan, D R Cornblath, J D Glass, et al.Journal of the American Academy of Dermatology|March 21, 2007
Immunohistochemical staining for CD45R isoforms in paraffin sections to diagnose mycosis fungoides-type cutaneous T-cell lymphomaSahar A Ismail, Rujing Han, Sharon L Sanborn, et al.Journal of Immunology (Baltimore, Md. : 1950)|December 2, 1998
Monocyte induction of IL-10 and down-regulation of IL-12 by iC3b deposited in ultraviolet-exposed human skinY Yoshida, K Kang, M Berger, et al.Genomics|November 1, 1989
Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophreniaT C Gilliam, N B Freimer, C A Kaufmann, et al.Cytogenetic and Genome Research|August 12, 2004
Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndromeM Tadin-Strapps, D Warburton, F A M Baumeister, et al.Genomics|April 1, 1992
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28G G Consalez, C L Stayton, N B Freimer, et al.Pageof 18