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Germline PTEN mutations are rare and highly penetrant
Cowden syndrome (multiple hamartoma syndrome, MIM 158350) is an early onset syndrome characterized by multiple hamartomas in the skin, mucous membranes, breast, thyroid and endometrium. Patients with Cowden syndrome have increased risk of breast cancer, thyroid cancer and endometrial cancer. In 1997...
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主要な著者: | , , , , , |
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フォーマット: | Artigo |
言語: | Inglês |
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BioMed Central
2006
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主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2837306/ https://ncbi.nlm.nih.gov/pubmed/20223021 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1897-4287-4-4-177 |
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