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British Journal of Rheumatology|May 1, 1993
Porphyria cutanea tarda associated with methotrexate therapyT O'Neill, J Simpson, S J Smyth, et al.European Journal of Biochemistry|December 15, 1987
Molecular cloning of cDNA for human complement component C1s. The complete amino acid sequenceC M Mackinnon, P E Carter, S J Smyth, et al.Human Genetics|April 1, 1992
Homozygous acute intermittent porphyria: compound heterozygosity for adjacent base transitions in the same codon of the porphobilinogen deaminase geneD H Llewellyn, S J Smyth, G H Elder, et al.The British Journal of Dermatology|July 1, 1993
Detection of latent variegate porphyria by fluorescence emission spectroscopy of plasmaC Long, S J Smyth, J Woolf, et al.Human Genetics|October 1, 1990
Acute intermittent porphyria caused by a C----T mutation that produces a stop codon in the porphobilinogen deaminase geneG A Scobie, D H Llewellyn, A J Urquhart, et al.Pageof 1