1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency by Linhares, Natália Duarte, Freire, Maíra Cristina Menezes, Cardenas, Raony Guimarães Corrêa do Carmo Lisboa, Pena, Heloisa Barbosa, Lachlan, Katherine, Dallapiccola, Bruno, Bacino, Carlos, Delobel, Bruno, James, Paul, Thuresson, Ann-Charlotte, Annerén, Göran, Pena, Sérgio D J

Get full text

Molecular characterization of beta-tubulin from Phakopsora pachyrhizi, the causal agent of Asian soybean rust by Maciel, Talles Eduardo Ferreira, Freire, Maíra Cristina Menezes, de Almeida, Alvaro M R, de Oliveira, Luiz Orlando

Get full text

Abstract A59: Impact of NGS four-gene panel in screening genes with potential therapies in NSCLC by Bustamante, Carolina, Freire, Maíra Cristina Menezes, Lopes, Natália Penido, Zalis, Mariano

Get full text

Abstract B50: Personna Onco: A multicancer panel for mutational screening in a Brazilian cohort by Freire, Maíra Cristina Menezes, Pereira, Michele Araújo, Cirillo, Priscila Daniele Ramos, Lopes, Natália Penido, Bustamante, Carolina, Guedes, Rafael Lucas Muniz, Zalis, Mariano

Get full text

Nucleotide polymorphism in the 5.8S nrDNA gene and internal transcribed spacers in Phakopsora pachyrhizi viewed from structural models by Freire, Maíra Cristina Menezes, Silva, Maria Roméria da, Zhang, Xuecheng, Almeida, Álvaro Manuel Rodrigues, Stacey, Gary, Oliveira, Luiz Orlando de

Get full text

Retrospective karyotype study in mentally retarded patients by Teixeira, Wellcy Gonçalves, Marques, Fabiana Kalina, Freire, Maíra Cristina Menezes

Get full text