## 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,
β¦ LIBER β¦
Various types of primary liver tumors occur in patients with germ-line mutations of the APC gene
β Scribed by Cetta, Francesco; Montalto, Giulia; Santoro, GiulioAniello; Gori, Monica; Zuckermann, Michele; Boldrini, Renata; Bosman, Cesare; Tomlison, Gail
- Book ID
- 122449632
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 191 KB
- Volume
- 118
- Category
- Article
- ISSN
- 0016-5085
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