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pro vyhledávání: '"Pereira, Kallen Rayane"'
Autor:
Ribeiro , Leila Braga, Fin , Lucas Grangeiro, Pereira, Kallen Rayane, Montenegro , Raylson Araujo, Ferreira , Ana Iara Costa, Nakashima , Fabiana, Lins , Cynthia, Martins , Antonio Carlos Sansevero, Sequeira , Bianca Jorge, Costa , Wagner Carmo
Publikováno v:
Health & Diversity Journal; Vol. 4 No. 1 (2020); 38-44
Health and Diversity; Vol. 4 Núm. 1 (2020); 38-44
Revista Saúde & Diversidade; v. 4 n. 1 (2020); 38-44
Health and Diversity; Vol. 4 Núm. 1 (2020); 38-44
Revista Saúde & Diversidade; v. 4 n. 1 (2020); 38-44
Introduction: The lack of specialized care for congenital malformations and a genetic diagnosis service makes it difficult to register and monitor cases. Objective: This work aimed to investigate the main genetic anomalies that affect individuals wit