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Cell Death & Disease|October 21, 2011
Caspase deficiency alters the murine gut microbiomeB M Brinkman, F Hildebrand, M Kubica, et al.European Journal of Human Genetics : EJHG|June 3, 1999
Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorderG R Verheyen, S M Villafuerte, J Del-Favero, et al.Journal of Neurogenetics|July 17, 1998
Identification of a Drosophila presenilin homologue: evidence of alternatively spliced formsG Marfany, J Del-Favero, R Valero, et al.Annals of Neurology|February 28, 2001
Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2EP De Jonghe, I Mersivanova, E Nelis, et al.Human Genetics|September 15, 2000
Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentationJ Del-Favero, D Goossens, P De Jonghe, et al.Transactions of the Royal Society of Tropical Medicine and Hygiene|April 5, 2000
Dengue: emergence as a global public health problem and prospects for controlM JacobsPostgraduate Medicine|June 1, 1994
Maintenance therapy for obstructive lung disease. How to achieve the best response with the fewest agentsM JacobsBiochemical Pharmacology|September 15, 1984
Mechanism of action of hydralazine on vascular smooth muscleM JacobsMolecular Psychiatry|June 21, 2007
Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish familiesT Venken, M Alaerts, D Souery, et al.Genomics|December 28, 1999
A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genesG Kuhlenbäumer, A Schirmacher, J Meuleman, et al.Pageof 250