Genotype‐phenotype correlation in 99 familial adenomatous polyposis patients: A prospective prevention protocol

por de Oliveira, Junea C., Viana, Danilo V., Zanardo, Cleyton, Santos, Erika M. M., de Paula, André E., Palmero, Edenir I., Rossi, Benedito M.
Publicado 2019

Oncogenetics service and the Brazilian public health system: the experience of a reference Cancer Hospital

por Palmero, Edenir I., Galvão, Henrique C.R., Fernandes, Gabriela C., de Paula, André E., Oliveira, Junea C., Souza, Cristiano P., Andrade, Carlos E., Romagnolo, Luis G.C., Volc, Sahlua, C., Maximiliano, Sabato, Cristina, Grasel, Rebeca, Mauad, Edmundo, Reis, Rui M., Michelli, Rodrigo A.D.
Publicado 2016

Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer

por Felicio, Paula S., Grasel, Rebeca S., Campacci, Natalia, de Paula, Andre E., Galvão, Henrique C. R., Torrezan, Giovana T., Sabato, Cristina S., Fernandes, Gabriela C., Souza, Cristiano P., Michelli, Rodrigo D., Andrade, Carlos E., Barros, Bruna Durães De Figueiredo, Matsushita, Marcus M., Revil, Timothée, Ragoussis, Jiannis, Couch, Fergus J., Hart, Steven N., Reis, Rui M., Melendez, Matias E., Tonin, Patricia N., Carraro, Dirce M., Palmero, Edenir I.
Publicado 2020