Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases
Quaio, Caio Robledo D'Angioli Costa, Moreira, Caroline Monaco, Novo‐Filho, Gil Monteiro, Sacramento‐Bobotis, Patricia Rossi, Groenner Penna, Michele, Perazzio, Sandro Felix, Dutra, Aurelio Pimenta, Silva, Rafael Alves, Santos, Monize Nakamoto Provisor, Arruda, Vanessa Yurie Nozaki, Freitas, Vanessa Galdeno, Pereira, Vinícius Ceola, Pintao, Maria Carolina, Fornari, Alexandre Ricardo dos Santos, Buzolin, Ana Lígia, Oku, Andre Yuji, Burger, Matheus, Ramalho, Rodrigo Fernandes, Marco Antonio, David Santos, Ferreira, Elisa Napolitano, Pereira, Otavio Jose Eulalio, Cantagalli, Vanessa Dionisio, Trindade, Ana Carolina Gomes, Sousa, Rafaela Rogerio Floriano, Reys Furuzawa, Cintia, Verzini, Fernanda, Matalhana, Shirley Dezan, Romano, Naiade, Paixão, Daniele, Olivati, Caroline, Spolador, Gustavo Marquezani, Maciel, Gustavo Arantes Rosa, Rocha, Viviane Zorzanelli, Miguelez, Javier, Carvalho, Mario Henrique Burlacchini, Souza, Alexandre Wagner Silva, Andrade, Luis Eduardo Coelho, Chauffaille, Maria de Lourdes, Perazzio, Aline dos Santos Borgo, Catelani, Ana Lucia Pereira Monteiro, Mitne‐Neto, Miguel, Kim, Chong Ae, Baratela, Wagner Antonio da Rosa
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.12.2020)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.12.2020)
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