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American Journal of Human Genetics|August 1, 1987
Familial inheritance of a DXS164 deletion mutation from a heterozygous femaleJ T Lanman, M A Pericak-Vance, R J Bartlett, et al.Neurology|July 1, 1995
Apolipoprotein E, survival in Alzheimer's disease patients, and the competing risks of death and Alzheimer's diseaseE H Corder, A M Saunders, W J Strittmatter, et al.Cell|August 14, 1987
Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomereT C Gilliam, R E Tanzi, J L Haines, et al.Genomics|August 1, 1989
Huntington disease: no evidence for locus heterogeneityP M Conneally, J L Haines, R E Tanzi, et al.Nature Genetics|June 1, 1994
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer diseaseE H Corder, A M Saunders, N J Risch, et al.Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer diseaseD E Schmechel, A M Saunders, W J Strittmatter, et al.Annals of Neurology|May 1, 1979
Debrancher deficiency: neuromuscular disorder in 5 adultsS DiMauro, G B Hartwig, A Hays, et al.Journal of Medical Genetics|August 1, 1989
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral diseaseT Siddique, H Roper, M A Pericak-Vance, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993
Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer diseaseW J Strittmatter, K H Weisgraber, D Y Huang, et al.American Journal of Human Genetics|August 1, 1992
Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.Pageof 37