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Artigo de periodico
Mutations in the Caveolin-3 gene: when are they pathogenic? (2001)
Paula, Flavia de; Vainzof, Mariz ; Bernardino, Andréa L. F.; McNally, Elizabeth; Kunkel, Louis M; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULA, Flavia de et al. Mutations in the Caveolin-3 gene: when are they pathogenic?. American Journal of Medical Genetics, v. 99, p. 303-307, 2001Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o. Acesso em: 27 ago. 2024.
APA
Paula, F. de, Vainzof, M., Bernardino, A. L. F., McNally, E., Kunkel, L. M., & Zatz, M. (2001). Mutations in the Caveolin-3 gene: when are they pathogenic? American Journal of Medical Genetics, 99, 303-307. doi:10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
NLM
Paula F de, Vainzof M, Bernardino ALF, McNally E, Kunkel LM, Zatz M. Mutations in the Caveolin-3 gene: when are they pathogenic? [Internet]. American Journal of Medical Genetics. 2001 ; 99 303-307.[citado 2024 ago. 27 ] Available from: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
Vancouver
Paula F de, Vainzof M, Bernardino ALF, McNally E, Kunkel LM, Zatz M. Mutations in the Caveolin-3 gene: when are they pathogenic? [Internet]. American Journal of Medical Genetics. 2001 ; 99 303-307.[citado 2024 ago. 27 ] Available from: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
Artigo de periodico
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome) (2000)
Sertié, Andréa Laurato; Sossi, Vittorio; Camargo, Ana Maria A; Zatz, Mayana ; Brahe, Christina; Passos-Bueno, Maria Rita
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERTIÉ, Andréa Laurato et al. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics, v. 9, n. 13, p. 2051-2058, 2000Tradução . . Acesso em: 27 ago. 2024.
APA
Sertié, A. L., Sossi, V., Camargo, A. M. A., Zatz, M., Brahe, C., & Passos-Bueno, M. R. (2000). Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics, 9( 13), 2051-2058.
NLM
Sertié AL, Sossi V, Camargo AMA, Zatz M, Brahe C, Passos-Bueno MR. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics. 2000 ; 9( 13): 2051-2058.[citado 2024 ago. 27 ]
Vancouver
Sertié AL, Sossi V, Camargo AMA, Zatz M, Brahe C, Passos-Bueno MR. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics. 2000 ; 9( 13): 2051-2058.[citado 2024 ago. 27 ]
Artigo de periodico
Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients (2000)
Nishimura, A L; Oliveira, J. R. M.; Matioli, Sergio Russo ; Brito-Marques, Paulo Roberto; Bahia, Valéria Santoro; Nitrini, Ricardo; Zatz, Mayana
Source: Molecular Psychiatry. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NISHIMURA, A L et al. Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients. Molecular Psychiatry, v. 5, p. 563-566, 2000Tradução . . Disponível em: https://doi.org/10.1038/sj.mp.4000767. Acesso em: 27 ago. 2024.
APA
Nishimura, A. L., Oliveira, J. R. M., Matioli, S. R., Brito-Marques, P. R., Bahia, V. S., Nitrini, R., & Zatz, M. (2000). Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients. Molecular Psychiatry, 5, 563-566. doi:10.1038/sj.mp.4000767
NLM
Nishimura AL, Oliveira JRM, Matioli SR, Brito-Marques PR, Bahia VS, Nitrini R, Zatz M. Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients [Internet]. Molecular Psychiatry. 2000 ; 5 563-566.[citado 2024 ago. 27 ] Available from: https://doi.org/10.1038/sj.mp.4000767
Vancouver
Nishimura AL, Oliveira JRM, Matioli SR, Brito-Marques PR, Bahia VS, Nitrini R, Zatz M. Analysis of the disease risk locus DXS1047 polymorphism in brazilian Alzheimer patients [Internet]. Molecular Psychiatry. 2000 ; 5 563-566.[citado 2024 ago. 27 ] Available from: https://doi.org/10.1038/sj.mp.4000767

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