ReP USP - Resultado da busca

Artigo de periodico
Bone marrow and peripheral blood globin chain synthesis in sickle cell beta thalassaemia (1986)
Costa, F F; Zago, M A
Source: Journal of Medical Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, F F e ZAGO, M A. Bone marrow and peripheral blood globin chain synthesis in sickle cell beta thalassaemia. Journal of Medical Genetics, v. 23, p. 25-55, 1986Tradução . . Disponível em: https://doi.org/10.1136/jmg.23.3.252. Acesso em: 24 abr. 2024.
APA
Costa, F. F., & Zago, M. A. (1986). Bone marrow and peripheral blood globin chain synthesis in sickle cell beta thalassaemia. Journal of Medical Genetics, 23, 25-55. doi:10.1136/jmg.23.3.252
NLM
Costa FF, Zago MA. Bone marrow and peripheral blood globin chain synthesis in sickle cell beta thalassaemia [Internet]. Journal of Medical Genetics. 1986 ;23 25-55.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.23.3.252
Vancouver
Costa FF, Zago MA. Bone marrow and peripheral blood globin chain synthesis in sickle cell beta thalassaemia [Internet]. Journal of Medical Genetics. 1986 ;23 25-55.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.23.3.252
Artigo de periodico
Tetrasomy 18p: tentative delineation of a syndrome (1983)
Batista, Denise Aparecida dos Santos; Vianna-Morgante, Angela M ; Richieri-Costa, Antonio
Source: Journal of Medical Genetics. Unidades: IB, HRAC
Subjects: ANORMALIDADES CROMOSSÔMICAS, ANORMALIDADES CONGÊNITAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISTA, Denise Aparecida dos Santos e VIANNA-MORGANTE, Angela M e RICHIERI-COSTA, Antonio. Tetrasomy 18p: tentative delineation of a syndrome. Journal of Medical Genetics, v. 20, n. 2, p. 144-147, 1983Tradução . . Disponível em: https://doi.org/10.1136/jmg.20.2.144. Acesso em: 24 abr. 2024.
APA
Batista, D. A. dos S., Vianna-Morgante, A. M., & Richieri-Costa, A. (1983). Tetrasomy 18p: tentative delineation of a syndrome. Journal of Medical Genetics, 20( 2), 144-147. doi:10.1136/jmg.20.2.144
NLM
Batista DA dos S, Vianna-Morgante AM, Richieri-Costa A. Tetrasomy 18p: tentative delineation of a syndrome [Internet]. Journal of Medical Genetics. 1983 ; 20( 2): 144-147.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.20.2.144
Vancouver
Batista DA dos S, Vianna-Morgante AM, Richieri-Costa A. Tetrasomy 18p: tentative delineation of a syndrome [Internet]. Journal of Medical Genetics. 1983 ; 20( 2): 144-147.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.20.2.144
Artigo de periodico
Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus (1981)
Zatz, Mayana ; Vianna-Morgante, Angela M ; Campos, Patrícia; Diament, Aron Judka
Source: Journal of Medical Genetics. Unidades: IB, FM
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. Journal of Medical Genetics, v. 18, p. 442-447, 1981Tradução . . Disponível em: https://doi.org/10.1136/jmg.18.6.442. Acesso em: 24 abr. 2024.
APA
Zatz, M., Vianna-Morgante, A. M., Campos, P., & Diament, A. J. (1981). Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. Journal of Medical Genetics, 18, 442-447. doi:10.1136/jmg.18.6.442
NLM
Zatz M, Vianna-Morgante AM, Campos P, Diament AJ. Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus [Internet]. Journal of Medical Genetics. 1981 ; 18 442-447.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.18.6.442
Vancouver
Zatz M, Vianna-Morgante AM, Campos P, Diament AJ. Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus [Internet]. Journal of Medical Genetics. 1981 ; 18 442-447.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.18.6.442
Artigo de periodico
Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q) (1978)
Vianna-Morgante, Angela M
Source: Journal of Medical Genetics. Unidade: IB
Assunto: DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIANNA-MORGANTE, Angela M. Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q). Journal of Medical Genetics, v. 15, p. 305-310, 1978Tradução . . Disponível em: https://doi.org/10.1136/jmg.15.4.305. Acesso em: 24 abr. 2024.
APA
Vianna-Morgante, A. M. (1978). Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q). Journal of Medical Genetics, 15, 305-310. doi:10.1136/jmg.15.4.305
NLM
Vianna-Morgante AM. Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q) [Internet]. Journal of Medical Genetics. 1978 ; 15 305-310.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.15.4.305
Vancouver
Vianna-Morgante AM. Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q) [Internet]. Journal of Medical Genetics. 1978 ; 15 305-310.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.15.4.305
Artigo de periodico
Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same family (1977)
Levisky, Ruth Blay; Vianna-Morgante, Angela M ; Frota-Pessoa, Oswaldo; Scaff, Milberto; Tsanaclis, Ana Maria Crous; Levy, José Antonio
Source: Journal of Medical Genetics. Unidades: IB, FM
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEVISKY, Ruth Blay et al. Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same family. Journal of Medical Genetics, v. 14, p. 51-53, 1977Tradução . . Disponível em: https://doi.org/10.1136/jmg.14.1.51. Acesso em: 24 abr. 2024.
APA
Levisky, R. B., Vianna-Morgante, A. M., Frota-Pessoa, O., Scaff, M., Tsanaclis, A. M. C., & Levy, J. A. (1977). Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same family. Journal of Medical Genetics, 14, 51-53. doi:10.1136/jmg.14.1.51
NLM
Levisky RB, Vianna-Morgante AM, Frota-Pessoa O, Scaff M, Tsanaclis AMC, Levy JA. Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same family [Internet]. Journal of Medical Genetics. 1977 ; 14 51-53.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.14.1.51
Vancouver
Levisky RB, Vianna-Morgante AM, Frota-Pessoa O, Scaff M, Tsanaclis AMC, Levy JA. Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same family [Internet]. Journal of Medical Genetics. 1977 ; 14 51-53.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.14.1.51
Artigo de periodico
X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg (1976)
Zatz, Mayana ; Penha-Serrano, Creuza; Otto, Paulo A
Source: Journal of Medical Genetics. Unidade: IB
Assunto: DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e PENHA-SERRANO, Creuza e OTTO, Paulo A. X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg. Journal of Medical Genetics, v. 13, n. 3, p. 217-222, 1976Tradução . . Disponível em: https://doi.org/10.1136/jmg.13.3.217. Acesso em: 24 abr. 2024.
APA
Zatz, M., Penha-Serrano, C., & Otto, P. A. (1976). X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg. Journal of Medical Genetics, 13( 3), 217-222. doi:10.1136/jmg.13.3.217
NLM
Zatz M, Penha-Serrano C, Otto PA. X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg [Internet]. Journal of Medical Genetics. 1976 ; 13( 3): 217-222.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.13.3.217
Vancouver
Zatz M, Penha-Serrano C, Otto PA. X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg [Internet]. Journal of Medical Genetics. 1976 ; 13( 3): 217-222.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.13.3.217
Artigo de periodico
Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18 (1976)
Vianna-Morgante, Angela M ; Nozaki, Maria José; Ortega, Claudio C.; Coates, Verônica; Yamamura, Ysao
Source: Journal of Medical Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIANNA-MORGANTE, Angela M et al. Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18. Journal of Medical Genetics, v. 13, p. 366-370, 1976Tradução . . Disponível em: https://doi.org/10.1136/jmg.13.5.366. Acesso em: 24 abr. 2024.
APA
Vianna-Morgante, A. M., Nozaki, M. J., Ortega, C. C., Coates, V., & Yamamura, Y. (1976). Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18. Journal of Medical Genetics, 13, 366-370. doi:10.1136/jmg.13.5.366
NLM
Vianna-Morgante AM, Nozaki MJ, Ortega CC, Coates V, Yamamura Y. Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18 [Internet]. Journal of Medical Genetics. 1976 ; 13 366-370.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.13.5.366
Vancouver
Vianna-Morgante AM, Nozaki MJ, Ortega CC, Coates V, Yamamura Y. Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18 [Internet]. Journal of Medical Genetics. 1976 ; 13 366-370.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.13.5.366
Artigo de periodico
Turner's syndrome and 46,X,i(Yq) karyotype (1974)
Magnelli, Norma C.; Vianna-Morgante, Angela M ; Frota-Pessoa, Oswaldo; Taboada-Lopez, Manuel Gonzalo
Source: Journal of Medical Genetics. Unidade: IB
Assunto: DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAGNELLI, Norma C. et al. Turner's syndrome and 46,X,i(Yq) karyotype. Journal of Medical Genetics, v. 11, p. 403-406, 1974Tradução . . Disponível em: https://doi.org/10.1136/jmg.11.4.403. Acesso em: 24 abr. 2024.
APA
Magnelli, N. C., Vianna-Morgante, A. M., Frota-Pessoa, O., & Taboada-Lopez, M. G. (1974). Turner's syndrome and 46,X,i(Yq) karyotype. Journal of Medical Genetics, 11, 403-406. doi:10.1136/jmg.11.4.403
NLM
Magnelli NC, Vianna-Morgante AM, Frota-Pessoa O, Taboada-Lopez MG. Turner's syndrome and 46,X,i(Yq) karyotype [Internet]. Journal of Medical Genetics. 1974 ; 11 403-406.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.11.4.403
Vancouver
Magnelli NC, Vianna-Morgante AM, Frota-Pessoa O, Taboada-Lopez MG. Turner's syndrome and 46,X,i(Yq) karyotype [Internet]. Journal of Medical Genetics. 1974 ; 11 403-406.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1136/jmg.11.4.403

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