Source: International Journal of Cardiology. Unidade: FM
Subjects: PÉ (ANORMALIDADES), DOENÇAS HEREDITÁRIAS, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, CARDIOPATIAS CONGÊNITAS, DEFEITOS DO SEPTO INTERATRIAL
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FARIA, Mário Henrique Girão et al. A novel TBX5 missense mutation (V263M) in a family with atrial septal defects and postaxial hexodactyly. International Journal of Cardiology, v. 130, p. 30-35, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.ijcard.2008.06.090. Acesso em: 03 out. 2024.APA
Faria, M. H. G., Rabenhorst, H. B., Pereira, A. da C., & Krieger, J. E. (2008). A novel TBX5 missense mutation (V263M) in a family with atrial septal defects and postaxial hexodactyly. International Journal of Cardiology, 130, 30-35. doi:10.1016/j.ijcard.2008.06.090NLM
Faria MHG, Rabenhorst HB, Pereira A da C, Krieger JE. A novel TBX5 missense mutation (V263M) in a family with atrial septal defects and postaxial hexodactyly [Internet]. International Journal of Cardiology. 2008 ; 130 30-35.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ijcard.2008.06.090Vancouver
Faria MHG, Rabenhorst HB, Pereira A da C, Krieger JE. A novel TBX5 missense mutation (V263M) in a family with atrial septal defects and postaxial hexodactyly [Internet]. International Journal of Cardiology. 2008 ; 130 30-35.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ijcard.2008.06.090