Mao M. de Ferro
AuthID: R-00G-829
1
TITLE: 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 Full Text
AUTHORS: Filipe, B; Baltazar, C; Albuquerque, C; Fragoso, S; Lage, P; Vitoriano, I; Mao M de Ferro; Claro, I; Rodrigues, P; Fidalgo, P; Chaves, P ; Cravo, M ; Nobre N Leitao;
PUBLISHED: 2009, SOURCE: CLINICAL GENETICS, VOLUME: 76, ISSUE: 3
AUTHORS: Filipe, B; Baltazar, C; Albuquerque, C; Fragoso, S; Lage, P; Vitoriano, I; Mao M de Ferro; Claro, I; Rodrigues, P; Fidalgo, P; Chaves, P ; Cravo, M ; Nobre N Leitao;
PUBLISHED: 2009, SOURCE: CLINICAL GENETICS, VOLUME: 76, ISSUE: 3
