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Germline PTEN mutations are rare and highly penetrant

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Figure

Table 1. International Cowden Syndrome Consortium operational criteria (version 2000) as given by Charis Eng [2]
Table 2. Clinical signs in all demonstrated and assumed mutation carriers in the six Cowden syndrome families with PTEN mutation
Table 2. Clinical signs in all demonstrated and assumed mutation carriers in the six Cowden syndrome families with PTEN mutation
Table 2. Clinical signs in all demonstrated and assumed mutation carriers in the six Cowden syndrome families with PTEN mutation
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