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Issue DateTitleAuthor(s)
2013WT1, WTX and CTNNB1 mutation analysis in 43 patients with sporadic Wilms' tumorCardoso, Leila Cabral de Almeida; Souza, Kelly de; Reis, Adriana Helena de Oliveira; Andrade, Raissa Coelho; Britto, Alberto; Lima, Maria Angelica de Faria Domingues de; Santos, Anna Cláudia Evangelista dos; Faria, Paulo Antonio Silvestre de; Ferman, Sima Esther; Abreu, Hector Nicolas Seuánez; Vargas, Fernando Regla
2014Association of TP53 Polymorphisms on the Risk of Wilms TumorAndrade, Raissa Coelho; Cardoso, Leila Cabral de Almeida; Ferman, Sima Esther; Faria, Paulo Antonio Silvestre de; Abreu, Hector Nicolas Seuánez; Achatz, Maria Isabel; Vargas, Fernando Regla
2004Identification of three novel RB1 mutations in Brazilian patients with retinoblastoma by “exon by exon” PCR mediated SSCP analysisBraggio, Esteban; Bonvicino, Cibele Rodrigues; Vargas, Fernando Regla; Ferman, Sima Esther; Eisenberg, Ana Lucia Amaral; Abreu, Hector Nicolas Seuánez
2008Hereditary retinoblastoma transmitted by maternal germline mosaicismBarbosa, Raquel da Hora; Vargas, Fernando Regla; Aguiar, Fernanda Carla Carlos de; Ferman, Sima Esther; Lucena, Evandro; Bonvicino, Cibele Rodrigues; Abreu, Hector Nicolas Seuánez
2012Constitutional and somatic methylation status of DMRH19 and KvDMR in Wilms tumor patientsCardoso, Leila Cabral de Almeida; Castaño, Jair Antonio Tenorio; Pereira, Hanna Soares; Lima, Maria Angelica de Faria Domingues de; Santos, Anna Cláudia Evangelista dos; Faria, Paulo Antonio Silvestre de; Ferman, Sima Esther; Abreu, Hector Nicolas Seuánez; Nevado, Julian; Almeida, José Carlos Cabral de; Lapunzina, Pablo; Vargas, Fernando Regla
2012Influence of MDM2 and MDM4 on development and survival in hereditary retinoblastomaReis, Adriana Helena de Oliveira; Carvalho, Ivna Néria Silva Ribamar de; Damasceno, Paula Batista de Sousa; Ferman, Sima Esther; Lucena, Evandro; Camelo, Jorge Santiago Lopez; Abreu, Hector Nicolas Seuánez; Vargas, Fernando Regla