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American Journal of Human Genetics|August 1, 1991
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytesR G Roberts, T F Barby, E Manners, et al.Genomics|August 1, 1990
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy geneS Abbs, R G Roberts, C G Mathew, et al.Prenatal Diagnosis|October 4, 2000
Numbers or words? A randomized controlled trial of presenting screen negative results to pregnant womenT M Marteau, G Saidi, S Goodburn, et al.Genomics|May 1, 1989
A method for generating hybrids containing nonselected fragments of human chromosomesF Benham, K Hart, J Crolla, et al.Lancet (London, England)|December 22, 1990
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNAR G Roberts, D R Bentley, T F Barby, et al.Journal of Public Health Medicine|January 29, 1999
Objectives of genetic counselling: differing views of purchasers, providers and usersS Michie, A Allanson, D Armstrong, et al.Annals of Human Genetics|October 1, 1977
Assignment of the DIA1 locus to chromosome 22R A Fisher, S Povey, M Bobrow, et al.Science (New York, N.Y.)|November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophyS B Malhotra, K A Hart, H J Klamut, et al.BMJ (Clinical Research Ed.)|June 12, 1993
Uptake of cystic fibrosis testing in primary care: supply push or demand pull?H Bekker, M Modell, G Denniss, et al.Journal of Medical Genetics|March 1, 1991
Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish populationE C Landels, I H Ellis, A H Fensom, et al.Pageof 423