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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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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2006
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| Assuntos: | |
| Acceso en liña: | 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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