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Human Genetics|June 1, 1988
Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's diseaseL A Farrer, B Bonne-Tamir, M Frydman, et al.Human Mutation|March 3, 1998
Novel ATP7B mutations causing Wilson disease in several Israeli ethnic groupsH Kalinsky, A Funes, A Zeldin, et al.American Journal of Human Genetics|July 1, 1987
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13A M Bowcock, L A Farrer, L L Cavalli-Sforza, et al.American Journal of Human Genetics|January 1, 1994
Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellitesA M Bowcock, J Tomfohrde, J Weissenbach, et al.American Journal of Human Genetics|May 23, 1998
Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3H Tamary, L Shalmon, H Shalev, et al.Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001
Distinctive genetic signatures in the Libyan JewsN A Rosenberg, E Woolf, J K Pritchard, et al.Alcoholism, Clinical and Experimental Research|June 1, 1996
DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism researchK K Kidd, A J Pakstis, C M Castiglione, et al.American Journal of Human Genetics|June 19, 1998
A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutationsS A Tishkoff, A Goldman, F Calafell, et al.American Journal of Human Genetics|October 1, 1993
Polymorphic microsatellites and Wilson disease (WD)E A Stewart, A White, J Tomfohrde, et al.American Journal of Human Genetics|December 1, 1995
Evolution of haplotypes at the DRD2 locusC M Castiglione, A S Deinard, W C Speed, et al.Pageof 3