Source: Brazilian Journal of Genetics = Revista Brasileira de Genetica. Conference titles: International Congress of Human Genetics. Unidades: IB, HRAC
Assunto: GENÉTICA MÉDICA
ABNT
PASSOS-BUENO, Maria Rita et al. Screening of c934g and c937g mutations among patients with craniosynostosis reveals two apert patients not caused by any of these mutations. Brazilian Journal of Genetics = Revista Brasileira de Genetica. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 05 set. 2024. , 1996APA
Passos-Bueno, M. R., Richieri-Costa, A., Otto, P. A., Kok, F., Sertie, A. L., Alonso, L., et al. (1996). Screening of c934g and c937g mutations among patients with craniosynostosis reveals two apert patients not caused by any of these mutations. Brazilian Journal of Genetics = Revista Brasileira de Genetica. Instituto de Biociências, Universidade de São Paulo.NLM
Passos-Bueno MR, Richieri-Costa A, Otto PA, Kok F, Sertie AL, Alonso L, Brunoni D, Ribeiro SFM, Ferreira MC. Screening of c934g and c937g mutations among patients with craniosynostosis reveals two apert patients not caused by any of these mutations. Brazilian Journal of Genetics = Revista Brasileira de Genetica. 1996 ;19( 2 suppl.): 246.[citado 2024 set. 05 ]Vancouver
Passos-Bueno MR, Richieri-Costa A, Otto PA, Kok F, Sertie AL, Alonso L, Brunoni D, Ribeiro SFM, Ferreira MC. Screening of c934g and c937g mutations among patients with craniosynostosis reveals two apert patients not caused by any of these mutations. Brazilian Journal of Genetics = Revista Brasileira de Genetica. 1996 ;19( 2 suppl.): 246.[citado 2024 set. 05 ]