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Human Mutation|January 1, 1994
Searching for the 1 in 2,400,000: a review of dystrophin gene point mutationsR G Roberts, R J Gardner, M BobrowGenomics|July 1, 1991
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCRC G Cole, P N Goodfellow, M Bobrow, et al.Genomics|October 1, 1996
Sequence and chromosomal location of a human homologue of LRPR1, an FSH primary response geneR G Roberts, E Kendall, D Vetrie, et al.Lancet (London, England)|January 30, 1993
Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophyS C Yau, R G Roberts, M Bobrow, et al.Genomics|December 1, 1992
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplificationC G Cole, K Patel, J Shipley, et al.Genomics|October 1, 1992
A random STS strategy for construction of YAC contigs spanning defined chromosomal regionsC G Cole, I Dunham, A J Coffey, et al.Journal of Molecular Biology|July 25, 1997
Expression of the dystrophin-related protein 2 (Drp2) transcript in the mouseA K Dixon, T M Tait, E A Campbell, et al.Genomics|January 1, 1994
A 6.5-Mb yeast artificial chromosome contig incorporating 33 DNA markers on the human X chromosome at Xq22D Vetrie, E Kendall, A Coffey, et al.Experimental and Clinical Immunogenetics|January 1, 1985
Heterochromatic chromosome variation and reproductive failureM BobrowPhilosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
The prevention and avoidance of genetic disease: summing upM BobrowPageof 26