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Genomics|April 1, 1996
No genetic effect of alpha1-antichymotrypsin in Alzheimer diseaseJ L Haines, M L Pritchard, A M Saunders, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 1, 1984
Autologous mixed lymphocyte reaction in patients with myasthenia gravis: correlation with disease activityS J Greenberg, C W Olanow, D V Dawson, et al.Annals of Neurology|October 23, 1997
Apolipoprotein E genotypes in a neuropathological series from the Consortium to Establish a Registry for Alzheimer's DiseaseK A Welsh-Bohmer, M Gearing, A M Saunders, et al.Journal of Neuroimmunology|November 1, 1993
Binding of IgG to amyloid beta A4 peptide via the heavy-chain hinge region with preservation of antigen bindingD Huang, M Martin, D Hu, et al.Human Mutation|January 1, 1994
Detecting prion protein gene mutations by denaturing gradient gel electrophoresisJ K Fink, M L Peacock, J T Warren, et al.American Journal of Medical Genetics|January 1, 1991
A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher diseaseV M Pratt, J A Trofatter, A Schinzel, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locusM Frydman, B Bonné-Tamir, L A Farrer, et al.Proceedings. Symposium on Computer Applications in Medical Care|January 1, 1991
Software support for Huntingtons disease researchP M Conneally, J M Gersting, J M Gray, et al.American Journal of Human Genetics|July 1, 1993
The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HDL A Farrer, L A Cupples, P Wiater, et al.Connective Tissue Research|January 1, 1993
Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15M Velinov, M Sarfarazi, K Young, et al.Pageof 37