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Matches in SemOpenAlex for { <https://semopenalex.org/work/W2017342802> ?p ?o ?g. }

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• W2017342802 abstract "Cowden's syndrome (CS) is a rare genodermatosis, of autosomal dominant inheritance and variable phenotype, principally characterized by the formation of hamartomas in various organs, including skin, thyroid, breast, brain, and gastrointestinal tract and by the increased risk for the development of malignancy. The present report details the features of a very rare presentation of Cowden's syndrome affecting not only the mouth and gastrointestinal mucosa but also the central nervous system." @default.
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• W2017342802 date "2005-05-01" @default.
• W2017342802 modified "2023-10-16" @default.
• W2017342802 title "Cowden's syndrome affecting the mouth, gastrointestinal, and central nervous system: A case report and review of the literature" @default.
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• W2017342802 doi "https://doi.org/10.1016/j.tripleo.2004.08.032" @default.
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