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The Journal of Experimental Medicine|February 1, 1989
Chromosomal organization of the human major histocompatibility complex class I gene familyB H Koller, D E Geraghty, R DeMars, et al.American Journal of Medical Genetics|September 15, 1991
Linkage of an Alzheimer disease susceptibility locus to markers on human chromosome 21L L Heston, H T Orr, S S Rich, et al.American Journal of Human Genetics|October 1, 1987
Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6S S Rich, P Wilkie, L Schut, et al.American Journal of Human Genetics|July 1, 1991
Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6pL P Ranum, L A Duvick, S S Rich, et al.American Journal of Medical Genetics|September 15, 1991
Protocol for genetic testing in Huntington disease: three years of experience in MinnesotaM A Nance, B S Leroy, H T Orr, et al.Human Molecular Genetics|March 1, 1995
A gene responsible for cavernous malformations of the brain maps to chromosome 7qJ Dubovsky, J M Zabramski, J Kurth, et al.Neurobiology of Disease|June 22, 2000
The ins and outs of a polyglutamine neurodegenerative disease: spinocerebellar ataxia type 1 (SCA1)H T OrrHuman Pathology|June 1, 1994
Unstable trinucleotide repeats and the diagnosis of neurodegenerative diseaseH T OrrCarcinogenesis|June 1, 1986
Modulation of mouse skin tumor promotion by dietary 13-cis-retinoic acid and alpha-difluoromethylornithineA K Verma, L Duvick, M AliPageof 27