Cowden disease (CD) is a rare, autosomal dominant inherited cancer syndrome characterized by multiple benign and malignant lesions in a wide spectrum of tissues. While individuals with CD have an increased risk of breast and thyroid neoplasms, the primary features of CD are hamartomas. The gene for
✦ LIBER ✦
The genetic basis of Cowden’s syndrome: three novel mutations in PTEN/MMAC1/TEP1
✍ Scribed by H. C. Tsou; Xiao Li Ping; Xiao Xun Xie; Alexandra C. Gruener; Hong Zhang; R. Nini; Karen Swisshelm; Virginia Sybert; Terry M. Diamond; Rebecca Sutphen; M. Peacocke
- Book ID
- 106136937
- Publisher
- Springer
- Year
- 1998
- Tongue
- English
- Weight
- 522 KB
- Volume
- 102
- Category
- Article
- ISSN
- 0340-6717
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