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Genomics|May 1, 1991
A genetic linkage map of human chromosome 5 with 60 RFLP lociB Weiffenbach, K Falls, A Bricker, et al.Genomics|March 1, 1992
Localization of the D5 dopamine receptor gene to human chromosome 4p15.1-p15.3, centromeric to the Huntington's disease locusJ H Eubanks, M Altherr, C Wagner-McPherson, et al.Human Molecular Genetics|October 1, 1996
The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD regionS T Winokur, U Bengtsson, J C Vargas, et al.Molecular and Cellular Probes|December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4B A Allitto, A I McClatchey, G Barnes, et al.Molecular and Cellular Biology|June 1, 1981
Homothallic mating type switching generates lethal chromosome breaks in rad52 strains of Saccharomyces cerevisiaeB Weiffenbach, J E HaberAmerican Journal of Human Genetics|October 1, 1991
Complex patterns of linkage disequilibrium in the Huntington disease regionM E MacDonald, C Lin, L Srinidhi, et al.Human Molecular Genetics|December 1, 1992
A novel G protein-coupled receptor kinase gene cloned from 4p16.3C Ambrose, M James, G Barnes, et al.Molecular and Cellular Biology|August 1, 1985
Homothallic switching of Saccharomyces cerevisiae mating type genes by using a donor containing a large internal deletionB Weiffenbach, J E HaberGenes & Development|September 1, 1990
abdA expression in Drosophila embryosF Karch, W Bender, B WeiffenbachChromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.Pageof 19