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Biochemical Genetics|October 1, 1980
Assignment to chromosome 16 of a gene necessary for the expression of human mitochondrial glutamate oxaloacetate transaminase (aspartate aminotransferase) (E.C. 2.6.1.1.)E Tolley, V van Heyningen, R Brown, et al.
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.
Cancer Immunology, Immunotherapy : CII|January 1, 1983
An HLA-DR negative acute leukaemia which stimulates MLC and CMC responsesG M Taylor, W Fergusson, P A Dyer, 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.
Human Genetics|July 1, 1991
Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency familiesP J Sinnott, C Costigan, P A Dyer, et al.
The Journal of Rheumatology|April 1, 1985
Clinical features, autoantibodies and HLA-DR antigens in rheumatoid arthritisK Walton, P A Dyer, D M Grennan, et al.
Genomics|May 1, 1989
A method for generating hybrids containing nonselected fragments of human chromosomesF Benham, K Hart, J Crolla, et al.
Tissue Antigens|September 1, 1984
Optimum cell numbers for mixed lymphocyte responses in hanging-drop microculturesG M Taylor, H Jones, G Hughes, 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.
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