## Abstract Lynch syndrome, an autosomal dominant cancer predisposition caused by mutations in DNA mismatch repair (MMR) genes, mainly mainly mutL homolog 1, OMIM 120436 (__MLH1__) and mutS homolog 2, OMIM 609309 (__MSH2__), encompasses a tumor spectrum including primarily gastrointestinal, endomet
An Evidence-Based Review on Surveillance for Lynch Syndrome
β Scribed by H. F. Vasen; W. H. de Vos tot Nederveen Cappel
- Book ID
- 106322610
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 142 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0012-3706
No coin nor oath required. For personal study only.
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