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Artigo de periodico
Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations (2004)
Coutinho, Gabriela; Mitui, Midori; Campbell, Catarina; Carvalho, Beatriz T. Costa; Nahas, Shareef; Sun, Xia; Huo, Yong; Lai, Chih-hung; Thorstenson, Yvonne; Tanouye, Robert; Raskin, Salmo; Kim, Chong Ae; Llerena Junior, Juan; Gatti, Richard A.
Fonte: American Journal of Medical Genetics. Unidade: FM
Assuntos: DOENÇAS DO SISTEMA NERVOSO (GENÉTICA), DOENÇAS DO SISTEMA NERVOSO CENTRAL (GENÉTICA), GENÉTICA MOLECULAR, FAMÍLIA, POLIMORFISMO, BRASIL
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ABNT
COUTINHO, Gabriela et al. Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations. American Journal of Medical Genetics, v. 126A, n. 1, p. 33-40, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20570. Acesso em: 23 out. 2025.
APA
Coutinho, G., Mitui, M., Campbell, C., Carvalho, B. T. C., Nahas, S., Sun, X., et al. (2004). Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations. American Journal of Medical Genetics, 126A( 1), 33-40. doi:10.1002/ajmg.a.20570
NLM
Coutinho G, Mitui M, Campbell C, Carvalho BTC, Nahas S, Sun X, Huo Y, Lai C-hung, Thorstenson Y, Tanouye R, Raskin S, Kim CA, Llerena Junior J, Gatti RA. Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations [Internet]. American Journal of Medical Genetics. 2004 ; 126A( 1): 33-40.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/ajmg.a.20570
Vancouver
Coutinho G, Mitui M, Campbell C, Carvalho BTC, Nahas S, Sun X, Huo Y, Lai C-hung, Thorstenson Y, Tanouye R, Raskin S, Kim CA, Llerena Junior J, Gatti RA. Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations [Internet]. American Journal of Medical Genetics. 2004 ; 126A( 1): 33-40.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/ajmg.a.20570
Artigo de periodico
Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families (2003)
Kliemann, Susana; Waetge, Ricardo T. L.; Suzuki, Oscar T.; Passos-Bueno, Maria Rita ; Rosemberg, Sergio
Fonte: American Journal of Medical Genetics. Unidades: FM, IB
Assuntos: OFTALMOPATIAS (IMUNOLOGIA), OFTALMOPATIAS (GENÉTICA), ANTICORPOS, BIOLOGIA MOLECULAR
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KLIEMANN, Susana et al. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families. American Journal of Medical Genetics, v. 119 A, n. 1, p. 15-19, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20070. Acesso em: 23 out. 2025.
APA
Kliemann, S., Waetge, R. T. L., Suzuki, O. T., Passos-Bueno, M. R., & Rosemberg, S. (2003). Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families. American Journal of Medical Genetics, 119 A( 1), 15-19. doi:10.1002/ajmg.a.20070
NLM
Kliemann S, Waetge RTL, Suzuki OT, Passos-Bueno MR, Rosemberg S. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families [Internet]. American Journal of Medical Genetics. 2003 ; 119 A( 1): 15-19.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/ajmg.a.20070
Vancouver
Kliemann S, Waetge RTL, Suzuki OT, Passos-Bueno MR, Rosemberg S. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families [Internet]. American Journal of Medical Genetics. 2003 ; 119 A( 1): 15-19.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/ajmg.a.20070
Artigo de periodico
Mandibulofacial dysostosis Bauru type syndrome: a new case (1999)
Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
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ABNT
CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine. Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, v. 86, n. 2, p. 199-201, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g. Acesso em: 23 out. 2025.
APA
Ceide, R. M. Z., & Guion-Almeida, M. L. (1999). Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, 86( 2), 199-201. doi:10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
NLM
Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
Vancouver
Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
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: 23 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. 23 ] 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. 23 ] Available from: https://doi.org/10.1002/ajmg.1320420407
Artigo de periodico
Postaxial acrofacial dysostosis: report on two patients (1992)
Pereira, S C S; Rocha, C M G; Guion-Almeida, Maria Leine; Richieri-Costa, A
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
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ABNT
PEREIRA, S C S et al. Postaxial acrofacial dysostosis: report on two patients. American Journal of Medical Genetics, v. 44, n. 3, p. 274-279, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320440303. Acesso em: 23 out. 2025.
APA
Pereira, S. C. S., Rocha, C. M. G., Guion-Almeida, M. L., & Richieri-Costa, A. (1992). Postaxial acrofacial dysostosis: report on two patients. American Journal of Medical Genetics, 44( 3), 274-279. doi:10.1002/ajmg.1320440303
NLM
Pereira SCS, Rocha CMG, Guion-Almeida ML, Richieri-Costa A. Postaxial acrofacial dysostosis: report on two patients [Internet]. American Journal of Medical Genetics. 1992 ; 44( 3): 274-279.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/ajmg.1320440303
Vancouver
Pereira SCS, Rocha CMG, Guion-Almeida ML, Richieri-Costa A. Postaxial acrofacial dysostosis: report on two patients [Internet]. American Journal of Medical Genetics. 1992 ; 44( 3): 274-279.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/ajmg.1320440303
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: 23 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. 23 ] 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. 23 ] 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: 23 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. 23 ] 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. 23 ] 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: 23 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. 23 ] 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. 23 ] 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: 23 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. 23 ] 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. 23 ] 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: 23 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. 23 ]
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. 23 ]
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: 23 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. 23 ]
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. 23 ]
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: 23 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. 23 ]
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. 23 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 23 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. 23 ] 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. 23 ] 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: 23 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. 23 ] 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. 23 ] 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
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: 23 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. 23 ] 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. 23 ] 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)
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: 23 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. 23 ] 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. 23 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 23 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. 23 ] 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. 23 ] 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: 23 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. 23 ]
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. 23 ]
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
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: 23 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. 23 ]
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. 23 ]
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
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: 23 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. 23 ] 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. 23 ] Available from: https://doi.org/10.1002/ajmg.1320240323

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