Genomic alteration in hereditary colorectal patients without mutations in mismatch repair genes

por Villacis, Rolando AR, Santos, Érika MM, Rossi, Benedito M, Carraro, Dirce M, Kowalski, Luiz P, Rogatto, Silvia R
Publicado 2013

Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: Case report

por Torrezan, Giovana T, da Silva, Felipe CC, Krepischi, Ana CV, Santos, Érika MM, de O Ferreira, Fábio, Rossi, Benedito M, Carraro, Dirce M
Publicado 2011

Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients

por Silva, Felipe C, Lisboa, Bianca CG, Figueiredo, Marcia CP, Torrezan, Giovana T, Santos, Érika MM, Krepischi, Ana C, Rossi, Benedito M, Achatz, Maria I, Carraro, Dirce M
Publicado 2014

Germline DNA copy number variation in familial and early-onset breast cancer

por Krepischi, Ana CV, Achatz, Maria Isabel W, Santos, Erika MM, Costa, Silvia S, Lisboa, Bianca CG, Brentani, Helena, Santos, Tiago M, Gonçalves, Amanda, Nóbrega, Amanda F, Pearson, Peter L, Vianna-Morgante, Angela M, Carraro, Dirce M, Brentani, Ricardo R, Rosenberg, Carla
Publicado 2012