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Review explores classic and novel genetic tests identifying DNA variants linked to disorders and risk factors.
Classic genetic tests indicate, either directly or indirectly, the presence of DNA variants associated with rare but highly penetrant disorders such as Huntington's disease or multiple endocrine neoplasia type 2. This article not only reviews these classic tests but also shows how novel genetic tests can reveal the presence of DNA variants that are more logically considered risk factors for a given condition.
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Wylie Burke (2002) studied this question.
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