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Artigo de periodico
The human y chromosome: racial variation and evolution (1980)
Monsalve, Maria Victoria; Erdtmann, B.; Otto, Paulo A ; Frota-Pessoa, Oswaldo
Source: Revista Brasileira de Genética. Unidade: IB
Assunto: VARIAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONSALVE, Maria Victoria et al. The human y chromosome: racial variation and evolution. Revista Brasileira de Genética, v. 4, p. 433-446, 1980Tradução . . Acesso em: 06 ago. 2024.
APA
Monsalve, M. V., Erdtmann, B., Otto, P. A., & Frota-Pessoa, O. (1980). The human y chromosome: racial variation and evolution. Revista Brasileira de Genética, 4, 433-446.
NLM
Monsalve MV, Erdtmann B, Otto PA, Frota-Pessoa O. The human y chromosome: racial variation and evolution. Revista Brasileira de Genética. 1980 ; 4 433-446.[citado 2024 ago. 06 ]
Vancouver
Monsalve MV, Erdtmann B, Otto PA, Frota-Pessoa O. The human y chromosome: racial variation and evolution. Revista Brasileira de Genética. 1980 ; 4 433-446.[citado 2024 ago. 06 ]
Artigo de periodico
Effect of age on the detection rate in Duchenne muscular dystrophy (1980)
Zatz, Mayana ; Otto, Paulo A
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e OTTO, Paulo A. Effect of age on the detection rate in Duchenne muscular dystrophy. Journal of the Neurological Sciences, v. 47, n. 3, p. 407-410, 1980Tradução . . Disponível em: https://doi.org/10.1016/0022-510X(80)90093-3. Acesso em: 06 ago. 2024.
APA
Zatz, M., & Otto, P. A. (1980). Effect of age on the detection rate in Duchenne muscular dystrophy. Journal of the Neurological Sciences, 47( 3), 407-410. doi:10.1016/0022-510X(80)90093-3
NLM
Zatz M, Otto PA. Effect of age on the detection rate in Duchenne muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1980 ; 47( 3): 407-410.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1016/0022-510X(80)90093-3
Vancouver
Zatz M, Otto PA. Effect of age on the detection rate in Duchenne muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1980 ; 47( 3): 407-410.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1016/0022-510X(80)90093-3
Artigo de periodico
H-Y antigen expression in a case of XX true hermaphroditism (1980)
Moreira Filho, C. A.; Otto, Priscila Guimarães; Mustacchi, Zan; Frota-Pessoa, Oswaldo; Otto, Paulo A
Source: Human Genetics. Unidade: IB
Assunto: HERMAFRODITISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA FILHO, C. A. et al. H-Y antigen expression in a case of XX true hermaphroditism. Human Genetics, v. 55, p. 309-314, 1980Tradução . . Disponível em: https://doi.org/10.1007/bf00290209. Acesso em: 06 ago. 2024.
APA
Moreira Filho, C. A., Otto, P. G., Mustacchi, Z., Frota-Pessoa, O., & Otto, P. A. (1980). H-Y antigen expression in a case of XX true hermaphroditism. Human Genetics, 55, 309-314. doi:10.1007/bf00290209
NLM
Moreira Filho CA, Otto PG, Mustacchi Z, Frota-Pessoa O, Otto PA. H-Y antigen expression in a case of XX true hermaphroditism [Internet]. Human Genetics. 1980 ; 55 309-314.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1007/bf00290209
Vancouver
Moreira Filho CA, Otto PG, Mustacchi Z, Frota-Pessoa O, Otto PA. H-Y antigen expression in a case of XX true hermaphroditism [Internet]. Human Genetics. 1980 ; 55 309-314.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1007/bf00290209
Artigo de periodico
The use of concomitant serum pyruvatek-kinase (PK) and creatine-phosphokinase (CPK) for carrier detection in Duchenne's muscular dystrophy through discriminant analysis (1980)
Zatz, Mayana ; Otto, Paulo A
Source: Journal of Neurological Sciences. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e OTTO, Paulo A. The use of concomitant serum pyruvatek-kinase (PK) and creatine-phosphokinase (CPK) for carrier detection in Duchenne's muscular dystrophy through discriminant analysis. Journal of Neurological Sciences, v. 47, n. 3, p. 411-417, 1980Tradução . . Disponível em: https://doi.org/10.1016/0022-510X(80)90094-5. Acesso em: 06 ago. 2024.
APA
Zatz, M., & Otto, P. A. (1980). The use of concomitant serum pyruvatek-kinase (PK) and creatine-phosphokinase (CPK) for carrier detection in Duchenne's muscular dystrophy through discriminant analysis. Journal of Neurological Sciences, 47( 3), 411-417. doi:10.1016/0022-510X(80)90094-5
NLM
Zatz M, Otto PA. The use of concomitant serum pyruvatek-kinase (PK) and creatine-phosphokinase (CPK) for carrier detection in Duchenne's muscular dystrophy through discriminant analysis [Internet]. Journal of Neurological Sciences. 1980 ; 47( 3): 411-417.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1016/0022-510X(80)90094-5
Vancouver
Zatz M, Otto PA. The use of concomitant serum pyruvatek-kinase (PK) and creatine-phosphokinase (CPK) for carrier detection in Duchenne's muscular dystrophy through discriminant analysis [Internet]. Journal of Neurological Sciences. 1980 ; 47( 3): 411-417.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1016/0022-510X(80)90094-5
Artigo de periodico
Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker) (1980)
Zatz, Mayana ; Shapiro, Larry J.; Campion, David; Kaback, Michael M.; Otto, Paulo A
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker). Journal of the Neurological Sciences, v. 46, n. 3, p. 267-279, 1980Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(80)90051-9. Acesso em: 06 ago. 2024.
APA
Zatz, M., Shapiro, L. J., Campion, D., Kaback, M. M., & Otto, P. A. (1980). Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker). Journal of the Neurological Sciences, 46( 3), 267-279. doi:10.1016/0022-510x(80)90051-9
NLM
Zatz M, Shapiro LJ, Campion D, Kaback MM, Otto PA. Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker) [Internet]. Journal of the Neurological Sciences. 1980 ; 46( 3): 267-279.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1016/0022-510x(80)90051-9
Vancouver
Zatz M, Shapiro LJ, Campion D, Kaback MM, Otto PA. Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker) [Internet]. Journal of the Neurological Sciences. 1980 ; 46( 3): 267-279.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1016/0022-510x(80)90051-9
Artigo de periodico
The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome (1980)
Otto, Paulo A ; Otto, Priscila Guimarães
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: SÍNDROME DE DOWN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OTTO, Paulo A e OTTO, Priscila Guimarães. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome. American Journal of Medical Genetics, v. 6, p. 145-152, 1980Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320060208. Acesso em: 06 ago. 2024.
APA
Otto, P. A., & Otto, P. G. (1980). The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome. American Journal of Medical Genetics, 6, 145-152. doi:10.1002/ajmg.1320060208
NLM
Otto PA, Otto PG. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome [Internet]. American Journal of Medical Genetics. 1980 ; 6 145-152.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1002/ajmg.1320060208
Vancouver
Otto PA, Otto PG. The importance of A'-d ridge count in dermatoglyphic diagnosis of the Ullrich-turner syndrome [Internet]. American Journal of Medical Genetics. 1980 ; 6 145-152.[citado 2024 ago. 06 ] Available from: https://doi.org/10.1002/ajmg.1320060208

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