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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: 30 abr. 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 abr. 30 ] 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 abr. 30 ] Available from: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
Artigo de periodico
Genetic counseling for childless women at risk for Duchenne muscular dystrophy (1999)
Eggers, Sabine; Pavanello, Rita de Cássia M.; Passos-Bueno, Maria Rita ; 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
EGGERS, Sabine et al. Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, v. 86, p. 447-453, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p. Acesso em: 30 abr. 2024.
APA
Eggers, S., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (1999). Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, 86, 447-453. doi:10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
NLM
Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
Vancouver
Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
Artigo de periodico-carta/editorial
Transposon-like element in the dystrophin gene. [Carta ao editor] (1993)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Vainzof, Mariz
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e PASSOS-BUENO, Maria Rita e VAINZOF, Mariz. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 30 abr. 2024. , 1993
APA
Zatz, M., Passos-Bueno, M. R., & Vainzof, M. (1993). Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Passos-Bueno MR, Vainzof M. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. 1993 ; 46( 5): 601.[citado 2024 abr. 30 ]
Vancouver
Zatz M, Passos-Bueno MR, Vainzof M. Transposon-like element in the dystrophin gene. [Carta ao editor]. American Journal of Medical Genetics. 1993 ; 46( 5): 601.[citado 2024 abr. 30 ]
Artigo de periodico-carta/editorial
Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern DNA deletion. [Carta ao editor] (1992)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Rapaport, Debora; Pavanello, Rita de Cássia M.; Zatz, Mayana ; Bulman, Dennis E.
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern DNA deletion. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 30 abr. 2024. , 1992
APA
Vainzof, M., Passos-Bueno, M. R., Rapaport, D., Pavanello, R. de C. M., Zatz, M., & Bulman, D. E. (1992). Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern DNA deletion. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Passos-Bueno MR, Rapaport D, Pavanello R de CM, Zatz M, Bulman DE. Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern DNA deletion. [Carta ao editor]. American Journal of Medical Genetics. 1992 ; 44( 3): 382-384.[citado 2024 abr. 30 ]
Vancouver
Vainzof M, Passos-Bueno MR, Rapaport D, Pavanello R de CM, Zatz M, Bulman DE. Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern DNA deletion. [Carta ao editor]. American Journal of Medical Genetics. 1992 ; 44( 3): 382-384.[citado 2024 abr. 30 ]
Artigo de periodico-carta/editorial
Duchenne-like muscular dystrophy in the arabs. [Carta ao editor] (1990)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Rapaport, Debora
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e PASSOS-BUENO, Maria Rita e RAPAPORT, Debora. Duchenne-like muscular dystrophy in the arabs. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 30 abr. 2024. , 1990
APA
Zatz, M., Passos-Bueno, M. R., & Rapaport, D. (1990). Duchenne-like muscular dystrophy in the arabs. [Carta ao editor]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Passos-Bueno MR, Rapaport D. Duchenne-like muscular dystrophy in the arabs. [Carta ao editor]. American Journal of Medical Genetics. 1990 ; 37( 2): 289.[citado 2024 abr. 30 ]
Vancouver
Zatz M, Passos-Bueno MR, Rapaport D. Duchenne-like muscular dystrophy in the arabs. [Carta ao editor]. American Journal of Medical Genetics. 1990 ; 37( 2): 289.[citado 2024 abr. 30 ]
Artigo de periodico
Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance (1989)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Rapaport, D
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e PASSOS-BUENO, Maria Rita e RAPAPORT, D. Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance. American Journal of Medical Genetics, v. 32, n. 3 , p. 407-10, 1989Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320320328. Acesso em: 30 abr. 2024.
APA
Zatz, M., Passos-Bueno, M. R., & Rapaport, D. (1989). Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance. American Journal of Medical Genetics, 32( 3 ), 407-10. doi:10.1002/ajmg.1320320328
NLM
Zatz M, Passos-Bueno MR, Rapaport D. Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance [Internet]. American Journal of Medical Genetics. 1989 ;32( 3 ): 407-10.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320320328
Vancouver
Zatz M, Passos-Bueno MR, Rapaport D. Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance [Internet]. American Journal of Medical Genetics. 1989 ;32( 3 ): 407-10.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320320328
Artigo de periodico
Relation between height and clinical course in duchenne muscular dystrophy (1988)
Zatz, Mayana ; Rapaport, D; Vainzof, Mariz ; Rocha, J M L; Pavanello, R C M; Colletto, G M D; Peres, C A
Source: American Journal of Medical Genetics. Unidades: ICB, IB
Subjects: DISTROFIA MUSCULAR, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Relation between height and clinical course in duchenne muscular dystrophy. American Journal of Medical Genetics, v. 29, p. 405-10, 1988Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320290223. Acesso em: 30 abr. 2024.
APA
Zatz, M., Rapaport, D., Vainzof, M., Rocha, J. M. L., Pavanello, R. C. M., Colletto, G. M. D., & Peres, C. A. (1988). Relation between height and clinical course in duchenne muscular dystrophy. American Journal of Medical Genetics, 29, 405-10. doi:10.1002/ajmg.1320290223
NLM
Zatz M, Rapaport D, Vainzof M, Rocha JML, Pavanello RCM, Colletto GMD, Peres CA. Relation between height and clinical course in duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1988 ;29 405-10.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320290223
Vancouver
Zatz M, Rapaport D, Vainzof M, Rocha JML, Pavanello RCM, Colletto GMD, Peres CA. Relation between height and clinical course in duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1988 ;29 405-10.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320290223
Artigo de periodico
Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophy (1988)
Zatz, Mayana ; Rapaport, Debora; Vainzof, Mariz ; Pavanello, Rita de Cássia M.; Rocha, Jane Maria Leite da; Betti, Roberto Tadeu Barcelos; Otto, Paulo A
Source: American Journal of Medical Genetics. 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. Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophy. American Journal of Medical Genetics, v. 31, n. 4, p. 821-833, 1988Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320310415. Acesso em: 30 abr. 2024.
APA
Zatz, M., Rapaport, D., Vainzof, M., Pavanello, R. de C. M., Rocha, J. M. L. da, Betti, R. T. B., & Otto, P. A. (1988). Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophy. American Journal of Medical Genetics, 31( 4), 821-833. doi:10.1002/ajmg.1320310415
NLM
Zatz M, Rapaport D, Vainzof M, Pavanello R de CM, Rocha JML da, Betti RTB, Otto PA. Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1988 ; 31( 4): 821-833.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320310415
Vancouver
Zatz M, Rapaport D, Vainzof M, Pavanello R de CM, Rocha JML da, Betti RTB, Otto PA. Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1988 ; 31( 4): 821-833.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320310415
Artigo de periodico
Effects of mazindol on growth hormone levels in patients with duchenne muscular dystrophy (1988)
Zatz, Mayana ; Rapaport, D; Vainzof, Mariz ; Pavanello, R C M; Rocha, J M L; Betti, R T B; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Effects of mazindol on growth hormone levels in patients with duchenne muscular dystrophy. American Journal of Medical Genetics, v. 31, n. 4 , p. 821-33, 1988Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320310415. Acesso em: 30 abr. 2024.
APA
Zatz, M., Rapaport, D., Vainzof, M., Pavanello, R. C. M., Rocha, J. M. L., Betti, R. T. B., & Otto, P. A. (1988). Effects of mazindol on growth hormone levels in patients with duchenne muscular dystrophy. American Journal of Medical Genetics, 31( 4 ), 821-33. doi:10.1002/ajmg.1320310415
NLM
Zatz M, Rapaport D, Vainzof M, Pavanello RCM, Rocha JML, Betti RTB, Otto PA. Effects of mazindol on growth hormone levels in patients with duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1988 ;31( 4 ): 821-33.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320310415
Vancouver
Zatz M, Rapaport D, Vainzof M, Pavanello RCM, Rocha JML, Betti RTB, Otto PA. Effects of mazindol on growth hormone levels in patients with duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1988 ;31( 4 ): 821-33.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320310415
Artigo de periodico
Genetic heterogeneity in duchenne muscular dystrophy (1987)
Zatz, Mayana ; Bortolini, E R
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DOENÇAS, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e BORTOLINI, E R. Genetic heterogeneity in duchenne muscular dystrophy. American Journal of Medical Genetics, v. 26, p. 237-40, 1987Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320260139. Acesso em: 30 abr. 2024.
APA
Zatz, M., & Bortolini, E. R. (1987). Genetic heterogeneity in duchenne muscular dystrophy. American Journal of Medical Genetics, 26, 237-40. doi:10.1002/ajmg.1320260139
NLM
Zatz M, Bortolini ER. Genetic heterogeneity in duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1987 ;26 237-40.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320260139
Vancouver
Zatz M, Bortolini ER. Genetic heterogeneity in duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1987 ;26 237-40.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320260139
Artigo de periodico
Azindol and growth hormone inhibition in duchenne muscular dystrophy (1987)
Zatz, Mayana ; Rapaport, D; Rocha, J M L; Pavanello, R C M; Betti, R T B
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Azindol and growth hormone inhibition in duchenne muscular dystrophy. American Journal of Medical Genetics, v. 27, n. 4 , p. 993-5, 1987Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320270433. Acesso em: 30 abr. 2024.
APA
Zatz, M., Rapaport, D., Rocha, J. M. L., Pavanello, R. C. M., & Betti, R. T. B. (1987). Azindol and growth hormone inhibition in duchenne muscular dystrophy. American Journal of Medical Genetics, 27( 4 ), 993-5. doi:10.1002/ajmg.1320270433
NLM
Zatz M, Rapaport D, Rocha JML, Pavanello RCM, Betti RTB. Azindol and growth hormone inhibition in duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1987 ;27( 4 ): 993-5.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320270433
Vancouver
Zatz M, Rapaport D, Rocha JML, Pavanello RCM, Betti RTB. Azindol and growth hormone inhibition in duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1987 ;27( 4 ): 993-5.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320270433
Artigo de periodico
Duchenne muscular dystrophy comparison among different racial groups (1987)
Bortolini, E R; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS, GRUPOS SOCIAIS (COMPARAÇÃO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BORTOLINI, E R e ZATZ, Mayana. Duchenne muscular dystrophy comparison among different racial groups. American Journal of Medical Genetics, v. 28, p. 925-9, 1987Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320280418. Acesso em: 30 abr. 2024.
APA
Bortolini, E. R., & Zatz, M. (1987). Duchenne muscular dystrophy comparison among different racial groups. American Journal of Medical Genetics, 28, 925-9. doi:10.1002/ajmg.1320280418
NLM
Bortolini ER, Zatz M. Duchenne muscular dystrophy comparison among different racial groups [Internet]. American Journal of Medical Genetics. 1987 ;28 925-9.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320280418
Vancouver
Bortolini ER, Zatz M. Duchenne muscular dystrophy comparison among different racial groups [Internet]. American Journal of Medical Genetics. 1987 ;28 925-9.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320280418
Artigo de periodico
Brief clinical report: Duchenne muscular dystrophy in a girl with a XXX/XX/X chromosomal constitution (1986)
Bortolini, E R; Martins da Silva, D; Chequer, R; Vianna-Morgante, Angela M ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, CROMOSSOMO X FRÁGIL, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BORTOLINI, E R et al. Brief clinical report: Duchenne muscular dystrophy in a girl with a XXX/XX/X chromosomal constitution. American Journal of Medical Genetics, v. 25, n. 2 , p. 239, 1986Tradução . . Acesso em: 30 abr. 2024.
APA
Bortolini, E. R., Martins da Silva, D., Chequer, R., Vianna-Morgante, A. M., & Zatz, M. (1986). Brief clinical report: Duchenne muscular dystrophy in a girl with a XXX/XX/X chromosomal constitution. American Journal of Medical Genetics, 25( 2 ), 239.
NLM
Bortolini ER, Martins da Silva D, Chequer R, Vianna-Morgante AM, Zatz M. Brief clinical report: Duchenne muscular dystrophy in a girl with a XXX/XX/X chromosomal constitution. American Journal of Medical Genetics. 1986 ;25( 2 ): 239.[citado 2024 abr. 30 ]
Vancouver
Bortolini ER, Martins da Silva D, Chequer R, Vianna-Morgante AM, Zatz M. Brief clinical report: Duchenne muscular dystrophy in a girl with a XXX/XX/X chromosomal constitution. American Journal of Medical Genetics. 1986 ;25( 2 ): 239.[citado 2024 abr. 30 ]
Artigo de periodico
Benign Duchenne muscular dystrophy in a patient with growth hormone deficienty: a five years follow-up (1986)
Zatz, Mayana ; Betti, R T B
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e BETTI, R T B. Benign Duchenne muscular dystrophy in a patient with growth hormone deficienty: a five years follow-up. American Journal of Medical Genetics, v. 24, p. 567-72, 1986Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320240323. Acesso em: 30 abr. 2024.
APA
Zatz, M., & Betti, R. T. B. (1986). Benign Duchenne muscular dystrophy in a patient with growth hormone deficienty: a five years follow-up. American Journal of Medical Genetics, 24, 567-72. doi:10.1002/ajmg.1320240323
NLM
Zatz M, Betti RTB. Benign Duchenne muscular dystrophy in a patient with growth hormone deficienty: a five years follow-up [Internet]. American Journal of Medical Genetics. 1986 ;24 567-72.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320240323
Vancouver
Zatz M, Betti RTB. Benign Duchenne muscular dystrophy in a patient with growth hormone deficienty: a five years follow-up [Internet]. American Journal of Medical Genetics. 1986 ;24 567-72.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320240323
Artigo de periodico
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis (1986)
Zatz, Mayana ; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS, ENZIMAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e OTTO, Paulo A. Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis. American Journal of Medical Genetics, v. 25, n. 2 , p. 219-31, 1986Tradução . . Acesso em: 30 abr. 2024.
APA
Zatz, M., & Otto, P. A. (1986). Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis. American Journal of Medical Genetics, 25( 2 ), 219-31.
NLM
Zatz M, Otto PA. Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis. American Journal of Medical Genetics. 1986 ;25( 2 ): 219-31.[citado 2024 abr. 30 ]
Vancouver
Zatz M, Otto PA. Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis. American Journal of Medical Genetics. 1986 ;25( 2 ): 219-31.[citado 2024 abr. 30 ]
Artigo de periodico
Investigation on genetic heterogeneity in Duchenne muscular dystrophy (1986)
Bortolini, E R; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, CROMOSSOMO X FRÁGIL, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BORTOLINI, E R e ZATZ, Mayana. Investigation on genetic heterogeneity in Duchenne muscular dystrophy. American Journal of Medical Genetics, v. 24, p. 111-7, 1986Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320240113. Acesso em: 30 abr. 2024.
APA
Bortolini, E. R., & Zatz, M. (1986). Investigation on genetic heterogeneity in Duchenne muscular dystrophy. American Journal of Medical Genetics, 24, 111-7. doi:10.1002/ajmg.1320240113
NLM
Bortolini ER, Zatz M. Investigation on genetic heterogeneity in Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1986 ;24 111-7.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320240113
Vancouver
Bortolini ER, Zatz M. Investigation on genetic heterogeneity in Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1986 ;24 111-7.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320240113
Artigo de periodico
Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study (1985)
Vainzof, Mariz ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz e ZATZ, Mayana. Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study. American Journal of Medical Genetics, v. 21, p. 395-8, 1985Tradução . . Acesso em: 30 abr. 2024.
APA
Vainzof, M., & Zatz, M. (1985). Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study. American Journal of Medical Genetics, 21, 395-8.
NLM
Vainzof M, Zatz M. Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study. American Journal of Medical Genetics. 1985 ;21 395-8.[citado 2024 abr. 30 ]
Vancouver
Vainzof M, Zatz M. Serum b-glucuronidase enxyme activity in progressive muscular dystrophies: a preliminary study. American Journal of Medical Genetics. 1985 ;21 395-8.[citado 2024 abr. 30 ]
Artigo de periodico
Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value? (1985)
Vainzof, Mariz ; Zatz, Mayana ; Otto, Paulo A
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz e ZATZ, Mayana e OTTO, Paulo A. Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value?. American Journal of Medical Genetics, v. 22, p. 81-7, 1985Tradução . . Acesso em: 30 abr. 2024.
APA
Vainzof, M., Zatz, M., & Otto, P. A. (1985). Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value? American Journal of Medical Genetics, 22, 81-7.
NLM
Vainzof M, Zatz M, Otto PA. Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value? American Journal of Medical Genetics. 1985 ;22 81-7.[citado 2024 abr. 30 ]
Vancouver
Vainzof M, Zatz M, Otto PA. Serum ck-mb activity in progressive muscular dystrophy: is it of nosologic value? American Journal of Medical Genetics. 1985 ;22 81-7.[citado 2024 abr. 30 ]
Artigo de periodico
Effects of genetic couseling on duchenne muscular dystrophy families in Brazil (1983)
Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, GENÉTICA MÉDICA, ACONSELHAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana. Effects of genetic couseling on duchenne muscular dystrophy families in Brazil. American Journal of Medical Genetics, v. 15, p. 483-490, 1983Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320150314. Acesso em: 30 abr. 2024.
APA
Zatz, M. (1983). Effects of genetic couseling on duchenne muscular dystrophy families in Brazil. American Journal of Medical Genetics, 15, 483-490. doi:10.1002/ajmg.1320150314
NLM
Zatz M. Effects of genetic couseling on duchenne muscular dystrophy families in Brazil [Internet]. American Journal of Medical Genetics. 1983 ; 15 483-490.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320150314
Vancouver
Zatz M. Effects of genetic couseling on duchenne muscular dystrophy families in Brazil [Internet]. American Journal of Medical Genetics. 1983 ; 15 483-490.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1002/ajmg.1320150314

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