Source: Molecular Genetics and Metabolism. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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GJETTING, Torben et al. A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics. Molecular Genetics and Metabolism, v. 73, p. 280-284, 2001Tradução . . Acesso em: 31 out. 2024.APA
Gjetting, T., Romstad, A., Haavik, J., Knappskog, P. M., Acosta, A. X., Silva Júnior, W. A. da, et al. (2001). A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics. Molecular Genetics and Metabolism, 73, 280-284.NLM
Gjetting T, Romstad A, Haavik J, Knappskog PM, Acosta AX, Silva Júnior WA da, Zago MA, Guldberg P, Güttler F. A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics. Molecular Genetics and Metabolism. 2001 ; 73 280-284.[citado 2024 out. 31 ]Vancouver
Gjetting T, Romstad A, Haavik J, Knappskog PM, Acosta AX, Silva Júnior WA da, Zago MA, Guldberg P, Güttler F. A phenylalanine Hydroxylase amino acid polymorphism with implications for meolecular diagnostics. Molecular Genetics and Metabolism. 2001 ; 73 280-284.[citado 2024 out. 31 ]
