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Environmental Science & Technology|May 15, 2019
Natural Chlordecone Degradation Revealed by Numerous Transformation Products Characterized in Key French West Indies Environmental CompartmentsMarion L Chevallier, Oriane Della-Negra, Sébastien Chaussonnerie, et al.Nature Genetics|November 4, 2000
Mutant WD-repeat protein in triple-A syndromeA Tullio-Pelet, R Salomon, S Hadj-Rabia, et al.Prenatal Diagnosis|February 4, 2015
Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasmaA Alberti, L J Salomon, M Le Lorc'h, et al.Nature Genetics|December 28, 1999
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegiaJ Hazan, N Fonknechten, D Mavel, et al.Plos One|March 20, 2008
Comparative analysis of Acinetobacters: three genomes for three lifestylesDavid Vallenet, Patrice Nordmann, Valérie Barbe, et al.Neurology|February 1, 1997
Machado-Joseph disease in four Chinese pedigrees: molecular analysis of 15 patients including two juvenile cases and clinical correlationsY X Zhou, Y Takiyama, S Igarashi, et al.Chemico-Biological Interactions|April 17, 2007
Extending the Bacillus cereus group genomics to putative food-borne pathogens of different toxicityAlla Lapidus, Eugene Goltsman, Sandrine Auger, et al.Cancer Research|September 15, 2000
Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumorsS E Russell, M A McIlhatton, J F Burrows, et al.Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.Pageof 46