ReP USP - Resultado da busca

Trabalho de evento-resumo
Analysis of five genes in brazilian patients with nonsyndromic mental retardation (2004)
Maranduba, Carlos Magno da Costa; Vianna-Morgante, Angela M ; Passos-Bueno, Maria Rita
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: RETARDO MENTAL, MUTAÇÃO GENÉTICA
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ABNT
MARANDUBA, Carlos Magno da Costa e VIANNA-MORGANTE, Angela M e PASSOS-BUENO, Maria Rita. Analysis of five genes in brazilian patients with nonsyndromic mental retardation. 2004, Anais.. Toronto: Instituto de Biociências, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Maranduba, C. M. da C., Vianna-Morgante, A. M., & Passos-Bueno, M. R. (2004). Analysis of five genes in brazilian patients with nonsyndromic mental retardation. In Abstracts. Toronto: Instituto de Biociências, Universidade de São Paulo.
NLM
Maranduba CM da C, Vianna-Morgante AM, Passos-Bueno MR. Analysis of five genes in brazilian patients with nonsyndromic mental retardation. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Maranduba CM da C, Vianna-Morgante AM, Passos-Bueno MR. Analysis of five genes in brazilian patients with nonsyndromic mental retardation. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo
Cellular responses to genotoxic stress induced by temozolomide in an astrocytic cell line (U343 MG-a) (2004)
Bahia, Marcelo de Oliveira; Bassi, Carmem Lúcia; Mello, S. S.; Cardoso, R. S.; Fachin, Ana Lúcia; Passos, Geraldo Aleixo Silva; Donadi, Eduardo Antônio; Carlotti Júnior, Carlos Gilberto; Sakamoto-Hojo, Elza Tiemi
Source: Program. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FORP, FMRP, FFCLRP
Assunto: GENÉTICA MÉDICA
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ABNT
BAHIA, Marcelo de Oliveira et al. Cellular responses to genotoxic stress induced by temozolomide in an astrocytic cell line (U343 MG-a). 2004, Anais.. Toronto: Faculdade de Odontologia de Ribeirão Preto, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Bahia, M. de O., Bassi, C. L., Mello, S. S., Cardoso, R. S., Fachin, A. L., Passos, G. A. S., et al. (2004). Cellular responses to genotoxic stress induced by temozolomide in an astrocytic cell line (U343 MG-a). In Program. Toronto: Faculdade de Odontologia de Ribeirão Preto, Universidade de São Paulo.
NLM
Bahia M de O, Bassi CL, Mello SS, Cardoso RS, Fachin AL, Passos GAS, Donadi EA, Carlotti Júnior CG, Sakamoto-Hojo ET. Cellular responses to genotoxic stress induced by temozolomide in an astrocytic cell line (U343 MG-a). Program. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Bahia M de O, Bassi CL, Mello SS, Cardoso RS, Fachin AL, Passos GAS, Donadi EA, Carlotti Júnior CG, Sakamoto-Hojo ET. Cellular responses to genotoxic stress induced by temozolomide in an astrocytic cell line (U343 MG-a). Program. 2004 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo
Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients (2004)
Varela, C.; Kok, Fernando; Setian, Nuvarte; Kim, C A; Koiffmann, Celia Priszkulnik
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FM, IB
Subjects: MUTAÇÃO GENÉTICA, DOENÇAS GENÉTICAS
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ABNT
VARELA, C. et al. Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients. 2004, Anais.. Toronto: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Varela, C., Kok, F., Setian, N., Kim, C. A., & Koiffmann, C. P. (2004). Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients. In Abstracts. Toronto: Faculdade de Medicina, Universidade de São Paulo.
NLM
Varela C, Kok F, Setian N, Kim CA, Koiffmann CP. Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Varela C, Kok F, Setian N, Kim CA, Koiffmann CP. Is the Prader-Willi syndrome phenotype related to molecular mechanisms? A study of 75 patients. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo
Mutations in the IRF6 gene in two patients with popliteal pterygium syndrome (2004)
Zechi-Ceide, R. M.; Guion-Almeida, Maria Leine; Kokitsu-Nakata, N. M.; Passos-Bueno, Maria Rita
Source: Resumo. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: HRAC, IB
Subjects: SÍNDROMES OROFACIODIGITAIS, MUTAÇÃO GENÉTICA
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ABNT
ZECHI-CEIDE, R. M. et al. Mutations in the IRF6 gene in two patients with popliteal pterygium syndrome. 2004, Anais.. Toronto: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Zechi-Ceide, R. M., Guion-Almeida, M. L., Kokitsu-Nakata, N. M., & Passos-Bueno, M. R. (2004). Mutations in the IRF6 gene in two patients with popliteal pterygium syndrome. In Resumo. Toronto: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo.
NLM
Zechi-Ceide RM, Guion-Almeida ML, Kokitsu-Nakata NM, Passos-Bueno MR. Mutations in the IRF6 gene in two patients with popliteal pterygium syndrome. Resumo. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Zechi-Ceide RM, Guion-Almeida ML, Kokitsu-Nakata NM, Passos-Bueno MR. Mutations in the IRF6 gene in two patients with popliteal pterygium syndrome. Resumo. 2004 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo
The Treacher Collins syndrome gene (TCOF1) promoter characterization (2004)
Masotti, C; Annelin-Correa, L. M.; Splendore, Alessandra; Barbosa, A.; Lins, C. J.; Brochado, S.; Félix, Têmis Maria; Sogayar, Mari Cleide ; Passos-Bueno, Maria Rita
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: IQ, IB
Subjects: DISOSTOSE MANDIBULOFACIAL, MUTAÇÃO GENÉTICA
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ABNT
MASOTTI, C et al. The Treacher Collins syndrome gene (TCOF1) promoter characterization. 2004, Anais.. Toronto: Instituto de Química, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Masotti, C., Annelin-Correa, L. M., Splendore, A., Barbosa, A., Lins, C. J., Brochado, S., et al. (2004). The Treacher Collins syndrome gene (TCOF1) promoter characterization. In Abstracts. Toronto: Instituto de Química, Universidade de São Paulo.
NLM
Masotti C, Annelin-Correa LM, Splendore A, Barbosa A, Lins CJ, Brochado S, Félix TM, Sogayar MC, Passos-Bueno MR. The Treacher Collins syndrome gene (TCOF1) promoter characterization. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Masotti C, Annelin-Correa LM, Splendore A, Barbosa A, Lins CJ, Brochado S, Félix TM, Sogayar MC, Passos-Bueno MR. The Treacher Collins syndrome gene (TCOF1) promoter characterization. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo
Expression and functional gene analysis in periosteal fibroblasts from Apert syndrome patients (2004)
Sertié, Andréa Laurato; Fanganiello, R. D.; Oliveira, N.; Cavalheiro, Sérgio; Alonso, N.; Passos-Bueno, Maria Rita
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: DESORDENS CRANIOMANDIBULARES, MUTAÇÃO GENÉTICA
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ABNT
SERTIÉ, Andréa Laurato et al. Expression and functional gene analysis in periosteal fibroblasts from Apert syndrome patients. 2004, Anais.. Toronto: Instituto de Biociências, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Sertié, A. L., Fanganiello, R. D., Oliveira, N., Cavalheiro, S., Alonso, N., & Passos-Bueno, M. R. (2004). Expression and functional gene analysis in periosteal fibroblasts from Apert syndrome patients. In Abstracts. Toronto: Instituto de Biociências, Universidade de São Paulo.
NLM
Sertié AL, Fanganiello RD, Oliveira N, Cavalheiro S, Alonso N, Passos-Bueno MR. Expression and functional gene analysis in periosteal fibroblasts from Apert syndrome patients. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Sertié AL, Fanganiello RD, Oliveira N, Cavalheiro S, Alonso N, Passos-Bueno MR. Expression and functional gene analysis in periosteal fibroblasts from Apert syndrome patients. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo
Möbius sequence: clinical and pathogenic analysis of 68 patients (2004)
Marques-Dias, Maria Joaquina; Paz, J. A.; Bertola, Débora R.; Albano, Lilian Maria José; Moreira, M. B.; Gonzalez, Claudette Hajaj; Kuczynski, Evelyn; Valente, M.; Kim, C. A.
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FM, IB
Subjects: DOENÇAS GENÉTICAS, LESÃO CEREBRAL CRÔNICA
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ABNT
MARQUES-DIAS, Maria Joaquina et al. Möbius sequence: clinical and pathogenic analysis of 68 patients. 2004, Anais.. Toronto: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Marques-Dias, M. J., Paz, J. A., Bertola, D. R., Albano, L. M. J., Moreira, M. B., Gonzalez, C. H., et al. (2004). Möbius sequence: clinical and pathogenic analysis of 68 patients. In Abstracts. Toronto: Faculdade de Medicina, Universidade de São Paulo.
NLM
Marques-Dias MJ, Paz JA, Bertola DR, Albano LMJ, Moreira MB, Gonzalez CH, Kuczynski E, Valente M, Kim CA. Möbius sequence: clinical and pathogenic analysis of 68 patients. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Marques-Dias MJ, Paz JA, Bertola DR, Albano LMJ, Moreira MB, Gonzalez CH, Kuczynski E, Valente M, Kim CA. Möbius sequence: clinical and pathogenic analysis of 68 patients. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo
Sequencing of the breakpoint junction fragments of an X; autosome translocation in a female with Duchenne muscular dystrophy (2004)
Vianna-Morgante, Angela M ; Kerkis, Irina E.; Krepischi, Ana Cristina Victorino
Source: Posters. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
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ABNT
VIANNA-MORGANTE, Angela M e KERKIS, Irina E. e KREPISCHI, Ana Cristina Victorino. Sequencing of the breakpoint junction fragments of an X; autosome translocation in a female with Duchenne muscular dystrophy. 2004, Anais.. Toronto: Instituto de Biociências, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Vianna-Morgante, A. M., Kerkis, I. E., & Krepischi, A. C. V. (2004). Sequencing of the breakpoint junction fragments of an X; autosome translocation in a female with Duchenne muscular dystrophy. In Posters. Toronto: Instituto de Biociências, Universidade de São Paulo.
NLM
Vianna-Morgante AM, Kerkis IE, Krepischi ACV. Sequencing of the breakpoint junction fragments of an X; autosome translocation in a female with Duchenne muscular dystrophy. Posters. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Vianna-Morgante AM, Kerkis IE, Krepischi ACV. Sequencing of the breakpoint junction fragments of an X; autosome translocation in a female with Duchenne muscular dystrophy. Posters. 2004 ;[citado 2024 nov. 04 ]
Trabalho de evento-resumo
Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly: screening for loss of heterozigosity in 9p and 11q regions (2004)
Jehee, Fernanda Sarquis; Johnson, D.; Abe, Kikue Terada; Alonso, L.; Alonso, N.; Kim, C.; Cavalcante, D.; Wall, S. A.; Boyd, S.; Jabs, E.; Wikie, A. O.; Passos-Bueno, Maria Rita
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANORMALIDADES CRANIOFACIAIS
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ABNT
JEHEE, Fernanda Sarquis et al. Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly: screening for loss of heterozigosity in 9p and 11q regions. 2004, Anais.. Toronto: Instituto de Biociências, Universidade de São Paulo, 2004. . Acesso em: 04 nov. 2024.
APA
Jehee, F. S., Johnson, D., Abe, K. T., Alonso, L., Alonso, N., Kim, C., et al. (2004). Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly: screening for loss of heterozigosity in 9p and 11q regions. In Abstracts. Toronto: Instituto de Biociências, Universidade de São Paulo.
NLM
Jehee FS, Johnson D, Abe KT, Alonso L, Alonso N, Kim C, Cavalcante D, Wall SA, Boyd S, Jabs E, Wikie AO, Passos-Bueno MR. Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly: screening for loss of heterozigosity in 9p and 11q regions. Abstracts. 2004 ;[citado 2024 nov. 04 ]
Vancouver
Jehee FS, Johnson D, Abe KT, Alonso L, Alonso N, Kim C, Cavalcante D, Wall SA, Boyd S, Jabs E, Wikie AO, Passos-Bueno MR. Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly: screening for loss of heterozigosity in 9p and 11q regions. Abstracts. 2004 ;[citado 2024 nov. 04 ]

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