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Artigo de periodico
Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2 (2001)
Gattaz, Wagner F; Frieboes, Ralf; Moises, Hans W.; Yang, Liu; Li, Tao; Liu, Xieche; Vetter, Peter; Macciardi, Fabio; Hwu, Hai G.; Henn, Fritz
Fonte: American Journal of Medical Genetics. Unidade: FM
Assuntos: FOSFOLIPÍDEOS, ESQUIZOFRENIA
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ABNT
GATTAZ, Wagner F et al. Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2. American Journal of Medical Genetics, v. 105, n. 3, p. 246-249, 2001Tradução . . Acesso em: 24 out. 2025.
APA
Gattaz, W. F., Frieboes, R., Moises, H. W., Yang, L., Li, T., Liu, X., et al. (2001). Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2. American Journal of Medical Genetics, 105( 3), 246-249.
NLM
Gattaz WF, Frieboes R, Moises HW, Yang L, Li T, Liu X, Vetter P, Macciardi F, Hwu HG, Henn F. Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2. American Journal of Medical Genetics. 2001 ; 105( 3): 246-249.[citado 2025 out. 24 ]
Vancouver
Gattaz WF, Frieboes R, Moises HW, Yang L, Li T, Liu X, Vetter P, Macciardi F, Hwu HG, Henn F. Lack of Association Between Schizophrenia and the phospholipase-'A ind 2' Genes cPLA2 and sPLA2. American Journal of Medical Genetics. 2001 ; 105( 3): 246-249.[citado 2025 out. 24 ]
Artigo de periodico
Short stature, mental retardation, eye anomalies, and cleft lip/palate (1992)
Richieri-Costa, A; Guion-Almeida, Maria Leine
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assunto: ODONTOLOGIA
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ABNT
RICHIERI-COSTA, A e GUION-ALMEIDA, Maria Leine. Short stature, mental retardation, eye anomalies, and cleft lip/palate. American Journal of Medical Genetics, v. 42, n. 4, p. 449-452, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320420407. Acesso em: 24 out. 2025.
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (1992). Short stature, mental retardation, eye anomalies, and cleft lip/palate. American Journal of Medical Genetics, 42( 4), 449-452. doi:10.1002/ajmg.1320420407
NLM
Richieri-Costa A, Guion-Almeida ML. Short stature, mental retardation, eye anomalies, and cleft lip/palate [Internet]. American Journal of Medical Genetics. 1992 ; 42( 4): 449-452.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320420407
Vancouver
Richieri-Costa A, Guion-Almeida ML. Short stature, mental retardation, eye anomalies, and cleft lip/palate [Internet]. American Journal of Medical Genetics. 1992 ; 42( 4): 449-452.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320420407
Artigo de periodico
New case of zimmermann-laband syndrome with mild mental retardation, asymmetry of limbs , and hypertrichosis (1988)
Pina Neto, J M; Soares, Lúcia Regina Martelli; Souza, A H O; Petean, E B L; Llorach Velludo, Maria Angeles Sanches; Freitas, A C; Ribas, José Paulo
Fonte: American Journal of Medical Genetics. Unidades: FORP, FMRP
Assunto: MEDICINA
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ABNT
PINA NETO, J M et al. New case of zimmermann-laband syndrome with mild mental retardation, asymmetry of limbs , and hypertrichosis. American Journal of Medical Genetics, v. 31, n. 3 , p. 691-5, 1988Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320310326. Acesso em: 24 out. 2025.
APA
Pina Neto, J. M., Soares, L. R. M., Souza, A. H. O., Petean, E. B. L., Llorach Velludo, M. A. S., Freitas, A. C., & Ribas, J. P. (1988). New case of zimmermann-laband syndrome with mild mental retardation, asymmetry of limbs , and hypertrichosis. American Journal of Medical Genetics, 31( 3 ), 691-5. doi:10.1002/ajmg.1320310326
NLM
Pina Neto JM, Soares LRM, Souza AHO, Petean EBL, Llorach Velludo MAS, Freitas AC, Ribas JP. New case of zimmermann-laband syndrome with mild mental retardation, asymmetry of limbs , and hypertrichosis [Internet]. American Journal of Medical Genetics. 1988 ;31( 3 ): 691-5.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320310326
Vancouver
Pina Neto JM, Soares LRM, Souza AHO, Petean EBL, Llorach Velludo MAS, Freitas AC, Ribas JP. New case of zimmermann-laband syndrome with mild mental retardation, asymmetry of limbs , and hypertrichosis [Internet]. American Journal of Medical Genetics. 1988 ;31( 3 ): 691-5.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320310326
Artigo de periodico
Congenital scalp skull defects with distal limb anomalies (Adams-Oliver Syndrome - Mckusick 100030): further suggestion of autosomal recessive inheritance (1988)
Koiffmann, Celia Priszkulnik ; Wajntal, Anita; Huyke, B J; Castro, R M
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: GENÉTICA, ANOMALIA CRANIOFACIAL
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ABNT
KOIFFMANN, Celia Priszkulnik et al. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver Syndrome - Mckusick 100030): further suggestion of autosomal recessive inheritance. American Journal of Medical Genetics, v. 29, p. 263-8, 1988Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320290203. Acesso em: 24 out. 2025.
APA
Koiffmann, C. P., Wajntal, A., Huyke, B. J., & Castro, R. M. (1988). Congenital scalp skull defects with distal limb anomalies (Adams-Oliver Syndrome - Mckusick 100030): further suggestion of autosomal recessive inheritance. American Journal of Medical Genetics, 29, 263-8. doi:10.1002/ajmg.1320290203
NLM
Koiffmann CP, Wajntal A, Huyke BJ, Castro RM. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver Syndrome - Mckusick 100030): further suggestion of autosomal recessive inheritance [Internet]. American Journal of Medical Genetics. 1988 ;29 263-8.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320290203
Vancouver
Koiffmann CP, Wajntal A, Huyke BJ, Castro RM. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver Syndrome - Mckusick 100030): further suggestion of autosomal recessive inheritance [Internet]. American Journal of Medical Genetics. 1988 ;29 263-8.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320290203
Artigo de periodico
Partial aniridia , cerebellar ataxia , and mental deficiency ( gillespie syndrome ) in two brothers (1988)
Wittig, E O; Moreira, C A; Freire-Maia, N; Vianna-Morgante, Angela M
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: DOENÇAS GENÉTICAS, GENÉTICA MÉDICA
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ABNT
WITTIG, E O et al. Partial aniridia , cerebellar ataxia , and mental deficiency ( gillespie syndrome ) in two brothers. American Journal of Medical Genetics, v. 30, p. 703-8, 1988Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320300302. Acesso em: 24 out. 2025.
APA
Wittig, E. O., Moreira, C. A., Freire-Maia, N., & Vianna-Morgante, A. M. (1988). Partial aniridia , cerebellar ataxia , and mental deficiency ( gillespie syndrome ) in two brothers. American Journal of Medical Genetics, 30, 703-8. doi:10.1002/ajmg.1320300302
NLM
Wittig EO, Moreira CA, Freire-Maia N, Vianna-Morgante AM. Partial aniridia , cerebellar ataxia , and mental deficiency ( gillespie syndrome ) in two brothers [Internet]. American Journal of Medical Genetics. 1988 ;30 703-8.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320300302
Vancouver
Wittig EO, Moreira CA, Freire-Maia N, Vianna-Morgante AM. Partial aniridia , cerebellar ataxia , and mental deficiency ( gillespie syndrome ) in two brothers [Internet]. American Journal of Medical Genetics. 1988 ;30 703-8.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320300302
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
Fonte: American Journal of Medical Genetics. Unidades: ICB, IB
Assuntos: DISTROFIA MUSCULAR, GENÉTICA MÉDICA
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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: 24 out. 2025.
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 2025 out. 24 ] 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 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320290223
Artigo de periodico
Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra) (1988)
Pavanello, R C M; Eigier, A; Otto, Paulo A
Fonte: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA
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ABNT
PAVANELLO, R C M e EIGIER, A e OTTO, Paulo A. Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra). American Journal of Medical Genetics, v. 29, n. 4 , p. 845-9, 1988Tradução . . Acesso em: 24 out. 2025.
APA
Pavanello, R. C. M., Eigier, A., & Otto, P. A. (1988). Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra). American Journal of Medical Genetics, 29( 4 ), 845-9.
NLM
Pavanello RCM, Eigier A, Otto PA. Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra). American Journal of Medical Genetics. 1988 ;29( 4 ): 845-9.[citado 2025 out. 24 ]
Vancouver
Pavanello RCM, Eigier A, Otto PA. Relationship between mayer-rokitansky-kuster (mrk) anomaly and hereditary renal adysplasia (hra). American Journal of Medical Genetics. 1988 ;29( 4 ): 845-9.[citado 2025 out. 24 ]
Artigo de periodico
Epilepsy and mental deficiency ( ramon syndrome ) with juvenile rheumatoide arthritis (1988)
Pina Neto, J M; Moreno, A F C; Velludo, A; Voltarelli, J C; Moura Ribeiro, M V L; Athay, J L
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assuntos: DOENÇAS CONGÊNITAS, ARTRITE REUMATOIDE JUVENIL, DEFICIÊNCIA MENTAL, EPILEPSIA
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ABNT
PINA NETO, J M et al. Epilepsy and mental deficiency ( ramon syndrome ) with juvenile rheumatoide arthritis. American Journal of Medical Genetics, v. 24, p. 433-41, 1988Tradução . . Acesso em: 24 out. 2025.
APA
Pina Neto, J. M., Moreno, A. F. C., Velludo, A., Voltarelli, J. C., Moura Ribeiro, M. V. L., & Athay, J. L. (1988). Epilepsy and mental deficiency ( ramon syndrome ) with juvenile rheumatoide arthritis. American Journal of Medical Genetics, 24, 433-41.
NLM
Pina Neto JM, Moreno AFC, Velludo A, Voltarelli JC, Moura Ribeiro MVL, Athay JL. Epilepsy and mental deficiency ( ramon syndrome ) with juvenile rheumatoide arthritis. American Journal of Medical Genetics. 1988 ;24 433-41.[citado 2025 out. 24 ]
Vancouver
Pina Neto JM, Moreno AFC, Velludo A, Voltarelli JC, Moura Ribeiro MVL, Athay JL. Epilepsy and mental deficiency ( ramon syndrome ) with juvenile rheumatoide arthritis. American Journal of Medical Genetics. 1988 ;24 433-41.[citado 2025 out. 24 ]
Artigo de periodico
Zimmermann-laband syndrome (a new case) (1988)
Pina Neto, J M; Freitas, A C; Ribas, José Paulo
Fonte: American Journal of Medical Genetics. Unidades: FORP, FMRP
Assunto: MEDICINA
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ABNT
PINA NETO, J M e FREITAS, A C e RIBAS, José Paulo. Zimmermann-laband syndrome (a new case). American Journal of Medical Genetics, v. 87, n. 482, p. 21-4, 1988Tradução . . Acesso em: 24 out. 2025.
APA
Pina Neto, J. M., Freitas, A. C., & Ribas, J. P. (1988). Zimmermann-laband syndrome (a new case). American Journal of Medical Genetics, 87( 482), 21-4.
NLM
Pina Neto JM, Freitas AC, Ribas JP. Zimmermann-laband syndrome (a new case). American Journal of Medical Genetics. 1988 ;87( 482): 21-4.[citado 2025 out. 24 ]
Vancouver
Pina Neto JM, Freitas AC, Ribas JP. Zimmermann-laband syndrome (a new case). American Journal of Medical Genetics. 1988 ;87( 482): 21-4.[citado 2025 out. 24 ]
Artigo de periodico
Genetic and environmental components of serum creatine kinase (ck) and pyruvate kinase (pk) in normal twins: implication for genetic risks estimates in duchenne muscular dystrophy carries (1988)
Rapaport, D; Colletto, G M D; Zatz, Mayana
Fonte: American Journal of Medical Genetics. Unidades: ICB, IB
Assunto: GENÉTICA
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ABNT
RAPAPORT, D e COLLETTO, G M D e ZATZ, Mayana. Genetic and environmental components of serum creatine kinase (ck) and pyruvate kinase (pk) in normal twins: implication for genetic risks estimates in duchenne muscular dystrophy carries. American Journal of Medical Genetics, v. 31, p. 291-8, 1988Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320310206. Acesso em: 24 out. 2025.
APA
Rapaport, D., Colletto, G. M. D., & Zatz, M. (1988). Genetic and environmental components of serum creatine kinase (ck) and pyruvate kinase (pk) in normal twins: implication for genetic risks estimates in duchenne muscular dystrophy carries. American Journal of Medical Genetics, 31, 291-8. doi:10.1002/ajmg.1320310206
NLM
Rapaport D, Colletto GMD, Zatz M. Genetic and environmental components of serum creatine kinase (ck) and pyruvate kinase (pk) in normal twins: implication for genetic risks estimates in duchenne muscular dystrophy carries [Internet]. American Journal of Medical Genetics. 1988 ;31 291-8.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320310206
Vancouver
Rapaport D, Colletto GMD, Zatz M. Genetic and environmental components of serum creatine kinase (ck) and pyruvate kinase (pk) in normal twins: implication for genetic risks estimates in duchenne muscular dystrophy carries [Internet]. American Journal of Medical Genetics. 1988 ;31 291-8.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320310206
Artigo de periodico
Genetic heterogeneity in duchenne muscular dystrophy (1987)
Zatz, Mayana ; Bortolini, E R
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: DOENÇAS, DISTROFIA MUSCULAR
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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: 24 out. 2025.
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 2025 out. 24 ] 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 2025 out. 24 ] 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
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: DISTROFIA MUSCULAR, DOENÇAS
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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: 24 out. 2025.
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 2025 out. 24 ] 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 2025 out. 24 ] 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
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS, GRUPOS SOCIAIS (COMPARAÇÃO)
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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: 24 out. 2025.
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 2025 out. 24 ] 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 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320280418
Artigo de periodico
Tibial hemimelia: report on 37 new cases, clinical and gentic considerations (1987)
Richieri-Costa, A; Ferrareto, I; Masiero, D; Silva, C R M
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assuntos: ANORMALIDADES MÚLTIPLAS, FENÓTIPOS, GENÉTICA MÉDICA
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ABNT
RICHIERI-COSTA, A et al. Tibial hemimelia: report on 37 new cases, clinical and gentic considerations. American Journal of Medical Genetics, v. 27, n. 4 , p. 867-84, 1987Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320270414. Acesso em: 24 out. 2025.
APA
Richieri-Costa, A., Ferrareto, I., Masiero, D., & Silva, C. R. M. (1987). Tibial hemimelia: report on 37 new cases, clinical and gentic considerations. American Journal of Medical Genetics, 27( 4 ), 867-84. doi:10.1002/ajmg.1320270414
NLM
Richieri-Costa A, Ferrareto I, Masiero D, Silva CRM. Tibial hemimelia: report on 37 new cases, clinical and gentic considerations [Internet]. American Journal of Medical Genetics. 1987 ;27( 4 ): 867-84.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320270414
Vancouver
Richieri-Costa A, Ferrareto I, Masiero D, Silva CRM. Tibial hemimelia: report on 37 new cases, clinical and gentic considerations [Internet]. American Journal of Medical Genetics. 1987 ;27( 4 ): 867-84.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320270414
Artigo de periodico
H-y typing by elisa in a 46,x,dic(y) (q11.2101) male: effects of a nonmosaic yp duplication (1987)
Moreira-Filho, Carlos Alberto; Wachtel, S. S.; Daniel, A.; Priest, J. H.
Fonte: American Journal of Medical Genetics. Unidade: ICB
Assuntos: IMUNOLOGIA, ELISA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA-FILHO, Carlos Alberto et al. H-y typing by elisa in a 46,x,dic(y) (q11.2101) male: effects of a nonmosaic yp duplication. American Journal of Medical Genetics, v. 26, p. 709-717, 1987Tradução . . Acesso em: 24 out. 2025.
APA
Moreira-Filho, C. A., Wachtel, S. S., Daniel, A., & Priest, J. H. (1987). H-y typing by elisa in a 46,x,dic(y) (q11.2101) male: effects of a nonmosaic yp duplication. American Journal of Medical Genetics, 26, 709-717.
NLM
Moreira-Filho CA, Wachtel SS, Daniel A, Priest JH. H-y typing by elisa in a 46,x,dic(y) (q11.2101) male: effects of a nonmosaic yp duplication. American Journal of Medical Genetics. 1987 ; 26 709-717.[citado 2025 out. 24 ]
Vancouver
Moreira-Filho CA, Wachtel SS, Daniel A, Priest JH. H-y typing by elisa in a 46,x,dic(y) (q11.2101) male: effects of a nonmosaic yp duplication. American Journal of Medical Genetics. 1987 ; 26 709-717.[citado 2025 out. 24 ]
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
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, CROMOSSOMO X FRÁGIL, GENÉTICA MÉDICA
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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: 24 out. 2025.
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 2025 out. 24 ]
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 2025 out. 24 ]
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
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: DISTROFIA MUSCULAR, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), DOENÇAS GENÉTICAS
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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: 24 out. 2025.
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 2025 out. 24 ] 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 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320240323
Artigo de periodico
Heterizygous cystinuria and urinary lithiasis (1986)
Giucliani, R; Ferrari, I; Greene, Lewis Joel
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assuntos: CISTINÚRIA, CÁLCULOS URINÁRIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIUCLIANI, R e FERRARI, I e GREENE, Lewis Joel. Heterizygous cystinuria and urinary lithiasis. American Journal of Medical Genetics, v. 22, p. 703-15, 1986Tradução . . Acesso em: 24 out. 2025.
APA
Giucliani, R., Ferrari, I., & Greene, L. J. (1986). Heterizygous cystinuria and urinary lithiasis. American Journal of Medical Genetics, 22, 703-15.
NLM
Giucliani R, Ferrari I, Greene LJ. Heterizygous cystinuria and urinary lithiasis. American Journal of Medical Genetics. 1986 ;22 703-15.[citado 2025 out. 24 ]
Vancouver
Giucliani R, Ferrari I, Greene LJ. Heterizygous cystinuria and urinary lithiasis. American Journal of Medical Genetics. 1986 ;22 703-15.[citado 2025 out. 24 ]
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
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: 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: 24 out. 2025.
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 2025 out. 24 ]
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 2025 out. 24 ]
Artigo de periodico
Treatment of duchenne muscular dystrophy with growth hormone inhibitors (1986)
Zatz, Mayana ; Betti, R T B; Frota-Pessoa, O
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: DISTROFIA MUSCULAR (TRATAMENTO), DOENÇAS GENÉTICAS, GENÉTICA, HORMÔNIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e BETTI, R T B e FROTA-PESSOA, O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors. American Journal of Medical Genetics, v. 24, p. 549-66, 1986Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320240322. Acesso em: 24 out. 2025.
APA
Zatz, M., Betti, R. T. B., & Frota-Pessoa, O. (1986). Treatment of duchenne muscular dystrophy with growth hormone inhibitors. American Journal of Medical Genetics, 24, 549-66. doi:10.1002/ajmg.1320240322
NLM
Zatz M, Betti RTB, Frota-Pessoa O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors [Internet]. American Journal of Medical Genetics. 1986 ;24 549-66.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320240322
Vancouver
Zatz M, Betti RTB, Frota-Pessoa O. Treatment of duchenne muscular dystrophy with growth hormone inhibitors [Internet]. American Journal of Medical Genetics. 1986 ;24 549-66.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.1320240322

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