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A wide variety of techniques are available for detecting disease‐causing mutations within human genes; this report provides a brief review of such procedures. Good communication and exchange of materials between the clinical genetics field and the Human Genome Initiative will benefit both.—Rossiter, B. J. F.; Caskey, C. T. Molecular studies of human genetic disease. FASEB J. 5: 21–27; 1991.
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Rossiter et al. (1991) studied this question.
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