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Neuroscience Letters|April 22, 2005
An autosomal genomic screen for dementia in an extended Amish familyA E Ashley-Koch, Y Shao, J B Rimmler, et al.Human Molecular Genetics|March 8, 2008
C3 R102G polymorphism increases risk of age-related macular degenerationKylee L Spencer, Lana M Olson, Brent M Anderson, et al.Genomics|April 1, 1989
Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease geneS V Cheng, G R Martin, J H Nadeau, et al.Annals of the New York Academy of Sciences|December 16, 1996
Early detection of Alzheimer's disease by combining apolipoprotein E and neuroimagingG W Small, S Komo, A La Rue, et al.The Journal of Surgical Research|March 29, 2023
Factors Associated With Triage Decisions in Older Adult Trauma Patients: Impact on Mortality and MorbidityKrista L Haines, Tracy Truong, Charles N Trujillo, et al.Genomics|August 1, 1989
Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17A G Menon, D H Ledbetter, D C Rich, et al.Science (New York, N.Y.)|February 20, 1987
The genetic defect causing familial Alzheimer's disease maps on chromosome 21P H St George-Hyslop, R E Tanzi, R J Polinsky, et al.American Journal of Human Genetics|January 1, 1989
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)B R Seizinger, G E Farmer, J L Haines, et al.Neuroscience Letters|August 11, 1998
No association of alpha1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patientsM P Bass, L H Yamaoka, W K Scott, et al.Genes and Immunity|May 23, 2003
Osteopontin polymorphisms and disease course in multiple sclerosisS Caillier, L F Barcellos, S E Baranzini, et al.Pageof 93