Showing results (61-70 of 140) with videos related to
Sort By:
Pageof 14
Nucleic Acids Research|December 21, 2004
CR-EST: a resource for crop ESTsC Künne, M Lange, T Funke, et al.Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|April 2, 1999
[Results of "cross-over implantation of Palmaz-stents" with cross-over sheaths]H J Steinkamp, D Scheinert, H Hettwer, et al.TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|July 25, 2007
Comparative effectiveness of sugar beet microsatellite markers isolated from genomic libraries and GenBank ESTs to map the sugar beet genomeV Laurent, P Devaux, T Thiel, et al.European Journal of Trauma and Emergency Surgery : Official Publication of the European Trauma Society|August 27, 2024
Is overweight a predictor for a more severe course of disease in cases of necrotizing fasciitis?Claudius Illg, Markus Denzinger, Katarzyna Rachunek, et al.American Journal of Medical Genetics. Part A|September 9, 2020
A novel splice variant expands the LAMC3-associated cortical phenotype to frontal only polymicrogyria and adult-onset epilepsyBurkhard S Kasper, Cornelia Kraus, Michael Schwarz, et al.The Journal of Neuropsychiatry and Clinical Neurosciences|December 19, 2001
Subtle prefrontal neuropathology in a pilot magnetic resonance spectroscopy study in patients with borderline personality disorderL T van Elst, T Thiel, B Hesslinger, et al.The Journal of Urology|February 1, 1995
Ureteral amyloid deposits of beta 2-microglobulin origin in both kidney recipients of 1 donorN P Buchholz, H Moch, T C Gasser, et al.Neuron|July 13, 1999
Processing of visually presented sentences in Mandarin and English studied with fMRIM W Chee, D Caplan, C S Soon, et al.European Journal of Medical Genetics|September 11, 2016
Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1Bernt Popp, Regina Trollmann, Christian Büttner, et al.BMC Musculoskeletal Disorders|November 22, 2019
Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: a case reportMatthias Türk, Armin M Nagel, Frank Roemer, et al.Pageof 14