DOI:
10.1055/s-00000012
Endoscopy
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References
Filipe B, Baltazar C, Albuquerque C et al.
APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.
Clin Genet 2009;
76: 242-255
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