## Abstract The Turcot syndrome (TS) is a rare, probably autosomal recessive, disorder characterized by development of primary neuroepithelial tumors of the central nervous system (CNS) and numerous adenomatous colorectal polyps. To examine the possible involvement of mutations of the __APC__ gene,
✦ LIBER ✦
Germ-line and Somatic Mutations of the APC Gene and/or ß Catenin Gene in the Occurrence of FAP Associated Thyroid Carcinoma
✍ Scribed by F. Cetta; A. Dhamo; G. Malagnino; L. Barellini
- Book ID
- 105979650
- Publisher
- Springer
- Year
- 2007
- Tongue
- English
- Weight
- 88 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0364-2313
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