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
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Turning the 10–23 DNAzyme On and Off with Light
✍ Scribed by Julia L. Richards; Garry K. Seward; Yu-Hsiu Wang; Ivan J. Dmochowski
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 278 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1439-4227
No coin nor oath required. For personal study only.
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