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Artigo de periodico
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases (1998)
Zatz, Mayana ; Sumita, Denilce; Campiotto, Simone; Canovas, Marta; Cerqueira, Antonia; Vainzof, Mariz ; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases. American Journal of Medical Genetics, v. 78, p. 361-365, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g. Acesso em: 29 set. 2024.
APA
Zatz, M., Sumita, D., Campiotto, S., Canovas, M., Cerqueira, A., Vainzof, M., & Passos-Bueno, M. R. (1998). Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases. American Journal of Medical Genetics, 78, 361-365. doi:10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g
NLM
Zatz M, Sumita D, Campiotto S, Canovas M, Cerqueira A, Vainzof M, Passos-Bueno MR. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases [Internet]. American Journal of Medical Genetics. 1998 ; 78 361-365.[citado 2024 set. 29 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g
Vancouver
Zatz M, Sumita D, Campiotto S, Canovas M, Cerqueira A, Vainzof M, Passos-Bueno MR. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases [Internet]. American Journal of Medical Genetics. 1998 ; 78 361-365.[citado 2024 set. 29 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g
Artigo de periodico
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers (1998)
Sumita, Denilce Ritsuko; Vainzof, Mariz ; Campiotto, Simone; Cerqueira, Antonia M; Canovas, Marta; Otto, Paulo A ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SUMITA, Denilce Ritsuko et al. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers. American Journal of Medical Genetics, v. 80, p. 356-361, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19981204)80:4%3C356::aid-ajmg10%3E3.3.co;2-f. Acesso em: 29 set. 2024.
APA
Sumita, D. R., Vainzof, M., Campiotto, S., Cerqueira, A. M., Canovas, M., Otto, P. A., et al. (1998). Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers. American Journal of Medical Genetics, 80, 356-361. doi:10.1002/(sici)1096-8628(19981204)80:4%3C356::aid-ajmg10%3E3.3.co;2-f
NLM
Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Canovas M, Otto PA, Passos-Bueno MR, Zatz M. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers [Internet]. American Journal of Medical Genetics. 1998 ; 80 356-361.[citado 2024 set. 29 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19981204)80:4%3C356::aid-ajmg10%3E3.3.co;2-f
Vancouver
Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Canovas M, Otto PA, Passos-Bueno MR, Zatz M. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers [Internet]. American Journal of Medical Genetics. 1998 ; 80 356-361.[citado 2024 set. 29 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19981204)80:4%3C356::aid-ajmg10%3E3.3.co;2-f
Artigo de periodico
A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation (1992)
Rapaport, Debora; Passos-Bueno, Maria Rita ; Takata, Reinaldo Issao; Campiotto, Simone; Eggers, Sabine; Vainzof, Mariz ; Makover, Adina; Nudel, Uri; Yaffe, David; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, RETARDO MENTAL, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAPAPORT, Debora et al. A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation. Neuromuscular Disorders, v. 2, n. 2, p. 117-120, 1992Tradução . . Disponível em: https://doi.org/10.1016/0960-8966(92)90043-6. Acesso em: 29 set. 2024.
APA
Rapaport, D., Passos-Bueno, M. R., Takata, R. I., Campiotto, S., Eggers, S., Vainzof, M., et al. (1992). A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation. Neuromuscular Disorders, 2( 2), 117-120. doi:10.1016/0960-8966(92)90043-6
NLM
Rapaport D, Passos-Bueno MR, Takata RI, Campiotto S, Eggers S, Vainzof M, Makover A, Nudel U, Yaffe D, Zatz M. A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation [Internet]. Neuromuscular Disorders. 1992 ; 2( 2): 117-120.[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/0960-8966(92)90043-6
Vancouver
Rapaport D, Passos-Bueno MR, Takata RI, Campiotto S, Eggers S, Vainzof M, Makover A, Nudel U, Yaffe D, Zatz M. A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation [Internet]. Neuromuscular Disorders. 1992 ; 2( 2): 117-120.[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/0960-8966(92)90043-6

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