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Brain Research|November 1, 1986
Human N-CAM gene: mapping to chromosome 11 by analysis of somatic cell hybrids with mouse and human cDNA probesF S Walsh, W Putt, J G Dickson, et al.Journal of Cellular Biochemistry|January 1, 1982
A monoclonal antibody to the human epidermal growth factor receptorM D Waterfield, E L Mayes, P Stroobant, et al.Neurogenetics|February 7, 2001
Evidence that allelic variants of the spinocerebellar ataxia type 2 gene influence susceptibility to multiple sclerosisJ Chataway, S Sawcer, F Coraddu, et al.Vox Sanguinis|January 1, 1987
WES, a 'new' infrequent blood group antigen in FinnsP Sistonen, H R Nevanlinna, K Virtaranta-Knowles, et al.Clinical Pharmacology and Therapeutics|May 1, 1977
Pharmacokinetics and concentration-effect relationships of intervenous and oral clonidineD S Davies, A M Wing, J L Reid, et al.Journal of Neuroimmunology|August 3, 1999
A screen of candidates from peaks of linkage: evidence for the involvement of myeloperoxidase in multiple sclerosisJ Chataway, S Sawcer, R Feakes, et al.Nature Genetics|August 1, 1996
A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22S Sawcer, H B Jones, R Feakes, et al.Genetic Epidemiology|May 14, 1999
Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosisR Feakes, S Sawcer, J Chataway, et al.Human Genetics|February 1, 1992
The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditismG D Berkovitz, P Y Fechner, S M Marcantonio, et al.Pageof 25