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Diabetologia|July 1, 1984
HLA antigens and risk factors for nephropathy in type 1 (insulin-dependent) diabetes mellitusC Walton, P A Dyer, J A Davidson, et al.Human Genetics|March 1, 1987
DNA deletions in mild and severe Becker muscular dystrophyK A Hart, S Hodgson, A Walker, et al.Lancet (London, England)|March 31, 1979
Amniotic-fluid acetylcholinesterase as a possible diagnostic test for neural-tube defects in early pregnancyA D Smith, N J Wald, H S Cuckle, 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.Arthritis and Rheumatism|August 1, 1988
Complement C4B-null alleles in Felty's syndromeW Thomson, P A Sanders, M Davis, et al.Transplantation|July 1, 1987
Posttransplant antidonor lymphocytotoxic antibody production in relation to graft outcomeS Martin, P A Dyer, N P Mallick, et al.Journal of Medical Genetics|March 1, 1987
The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophyS Hodgson, A Walker, C Cole, et al.Neuromuscular Disorders : NMD|January 1, 1992
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental abilityS V Hodgson, S Abbs, S Clark, et al.The EMBO Journal|May 1, 1989
Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypesS Collier, P J Sinnott, P A Dyer, et al.Journal of Medical Genetics|December 1, 1985
Immunogenetic studies in families with rheumatoid arthritis and autoimmune thyroid diseaseP A Sanders, D M Grennan, P A Dyer, et al.Pageof 22