QUEDAS, Elisangela P. S.; LONGUINI, Viviane C.; SEKIYA, Tomoko; COUTINHO, Flavia L.; TOLEDO, Sergio P. A.; TANNURI, Uenis; TOLEDO, Rodrigo A. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family. Clinics, São Paulo, Brasil, v. 67, n. supl.1, p. 57–61, 2012. DOI: 10.6061/clinics/2012(Sup01)11. Disponível em: https://revistas.usp.br/clinics/article/view/19722.. Acesso em: 23 jul. 2024.