Search Results - Scottolini, A G

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  1. 1
    A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia

    A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia by Petersen, C E, Scottolini, A G, Cody, L R, Mandel, M, Reimer, N, Bhagavan, N V

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  2. 2
    Effect of hyperglycaemia as assessed by glycosylated haemoglobin concentrations on red cell enzyme activities in diabetes mellitus

    Effect of hyperglycaemia as assessed by glycosylated haemoglobin concentrations on red cell enzyme activities in diabetes mellitus by Sorensen, S K, Scottolini, A G, Bhagavan, N V

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