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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.Annals of Clinical Biochemistry|November 1, 1978
Serum deoxycytidylate deaminase activity after myocardial infarctionR G Roberts, A G Davies, D D JonesNucleic Acids Research|August 11, 1989
Detection of novel genetic markers by mismatch analysisR G Roberts, A J Montandon, M Bobrow, 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|August 1, 1992
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCRR G Roberts, A J Coffey, M Bobrow, et al.European Journal of Clinical Investigation|September 27, 2003
Effect of insulin upon protein degradation in cultured human myocytesR G Roberts, C P F Redfern, T H J GoodshipNeuroreport|July 31, 1995
Nicotinic acetylcholine receptors on capsaicin-sensitive nervesR G Roberts, J E Stevenson, R A Westerman, et al.Genomics|May 1, 1993
Exon structure of the human dystrophin geneR G Roberts, A J Coffey, M Bobrow, et al.Human Molecular Genetics|January 1, 1993
Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCRR A Gibson, M Buchwald, R G Roberts, et al.Genomics|November 5, 1997
Exon-intron organization of the human dystrophin geneC Nobile, J Marchi, V Nigro, et al.Pageof 8