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Trabalho de evento-resumo periodico
Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate? (1999)
Gaspar, D A; Pavanello, R C M; André, M; Steman, S; Zatz, Mayana ; Wyszynski, Diego F; Matioli, Sergio Russo ; Passos-Bueno, Maria Rita
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidades: FO, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GASPAR, D A et al. Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate?. American Journal of Human Genetics. San Francisco: Faculdade de Odontologia, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 1999
APA
Gaspar, D. A., Pavanello, R. C. M., André, M., Steman, S., Zatz, M., Wyszynski, D. F., et al. (1999). Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate? American Journal of Human Genetics. San Francisco: Faculdade de Odontologia, Universidade de São Paulo.
NLM
Gaspar DA, Pavanello RCM, André M, Steman S, Zatz M, Wyszynski DF, Matioli SR, Passos-Bueno MR. Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate? American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Vancouver
Gaspar DA, Pavanello RCM, André M, Steman S, Zatz M, Wyszynski DF, Matioli SR, Passos-Bueno MR. Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate? American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Trabalho de evento-resumo periodico
Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients (1999)
Paula, F de; Vainzof, Mariz ; McNally, E E; Kunkel, L M; Zatz, Mayana
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULA, F de et al. Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 1999
APA
Paula, F. de, Vainzof, M., McNally, E. E., Kunkel, L. M., & Zatz, M. (1999). Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.
NLM
Paula F de, Vainzof M, McNally EE, Kunkel LM, Zatz M. Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Vancouver
Paula F de, Vainzof M, McNally EE, Kunkel LM, Zatz M. Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Trabalho de evento-resumo periodico
Partial 'alfa'-sarcoglycan ('alfa'-SG) deficiency associated with the retention of the SG complex in a LGMD2D family (1999)
Vainzof, Mariz ; Moreira, E S; Canovas, M; Suzuki, Oscar T; Pavanello, Rita de Cássia M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Partial 'alfa'-sarcoglycan ('alfa'-SG) deficiency associated with the retention of the SG complex in a LGMD2D family. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 1999
APA
Vainzof, M., Moreira, E. S., Canovas, M., Suzuki, O. T., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (1999). Partial 'alfa'-sarcoglycan ('alfa'-SG) deficiency associated with the retention of the SG complex in a LGMD2D family. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Moreira ES, Canovas M, Suzuki OT, Pavanello R de CM, Passos-Bueno MR, Zatz M. Partial 'alfa'-sarcoglycan ('alfa'-SG) deficiency associated with the retention of the SG complex in a LGMD2D family. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Vancouver
Vainzof M, Moreira ES, Canovas M, Suzuki OT, Pavanello R de CM, Passos-Bueno MR, Zatz M. Partial 'alfa'-sarcoglycan ('alfa'-SG) deficiency associated with the retention of the SG complex in a LGMD2D family. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Trabalho de evento-resumo periodico
Association of specific mutations and severe mental retardation in Duchenne patients (1999)
Gomes, R R; Torres, A F B; Vainzof, Mariz ; Cerqueira, A M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, R R et al. Association of specific mutations and severe mental retardation in Duchenne patients. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 1999
APA
Gomes, R. R., Torres, A. F. B., Vainzof, M., Cerqueira, A. M., Passos-Bueno, M. R., & Zatz, M. (1999). Association of specific mutations and severe mental retardation in Duchenne patients. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.
NLM
Gomes RR, Torres AFB, Vainzof M, Cerqueira AM, Passos-Bueno MR, Zatz M. Association of specific mutations and severe mental retardation in Duchenne patients. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Vancouver
Gomes RR, Torres AFB, Vainzof M, Cerqueira AM, Passos-Bueno MR, Zatz M. Association of specific mutations and severe mental retardation in Duchenne patients. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Trabalho de evento-resumo periodico
A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family (1999)
Passos-Bueno, Maria Rita ; Wilcox, William R; Alonso, N.; Alonso, Luís G
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 1999
APA
Passos-Bueno, M. R., Wilcox, W. R., Alonso, N., & Alonso, L. G. (1999). A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.
NLM
Passos-Bueno MR, Wilcox WR, Alonso N, Alonso LG. A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Vancouver
Passos-Bueno MR, Wilcox WR, Alonso N, Alonso LG. A mild form of autosomal recessive craniotubular dyplasia in a large inbred brazilian family. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Trabalho de evento-resumo periodico
Physical mapping of the candidate region for the gene causing Limb-Girdle muscular dystrophy type 2G (LGMD2G) (1999)
Moreira, E S; Wiltshire, T; Vainzof, Mariz ; Reeves, R H; Zatz, Mayana ; Passos-Bueno, Maria Rita
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, E S et al. Physical mapping of the candidate region for the gene causing Limb-Girdle muscular dystrophy type 2G (LGMD2G). American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 1999
APA
Moreira, E. S., Wiltshire, T., Vainzof, M., Reeves, R. H., Zatz, M., & Passos-Bueno, M. R. (1999). Physical mapping of the candidate region for the gene causing Limb-Girdle muscular dystrophy type 2G (LGMD2G). American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.
NLM
Moreira ES, Wiltshire T, Vainzof M, Reeves RH, Zatz M, Passos-Bueno MR. Physical mapping of the candidate region for the gene causing Limb-Girdle muscular dystrophy type 2G (LGMD2G). American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Vancouver
Moreira ES, Wiltshire T, Vainzof M, Reeves RH, Zatz M, Passos-Bueno MR. Physical mapping of the candidate region for the gene causing Limb-Girdle muscular dystrophy type 2G (LGMD2G). American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Trabalho de evento-resumo periodico
Human type XVIII collagen (Col18A1) gene: structural organization, identification of new SNPs, and its exclusion as the Knobloch syndrome gene (1999)
Sertie, A L; Sossi, V; Passos-Bueno, Maria Rita ; Brahe, C
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERTIE, A L et al. Human type XVIII collagen (Col18A1) gene: structural organization, identification of new SNPs, and its exclusion as the Knobloch syndrome gene. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 1999
APA
Sertie, A. L., Sossi, V., Passos-Bueno, M. R., & Brahe, C. (1999). Human type XVIII collagen (Col18A1) gene: structural organization, identification of new SNPs, and its exclusion as the Knobloch syndrome gene. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.
NLM
Sertie AL, Sossi V, Passos-Bueno MR, Brahe C. Human type XVIII collagen (Col18A1) gene: structural organization, identification of new SNPs, and its exclusion as the Knobloch syndrome gene. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Vancouver
Sertie AL, Sossi V, Passos-Bueno MR, Brahe C. Human type XVIII collagen (Col18A1) gene: structural organization, identification of new SNPs, and its exclusion as the Knobloch syndrome gene. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Trabalho de evento-resumo periodico
Characterization of TCOF1 mutations in Brazilian patients affected with treacher Collins syndrome (1999)
Splendore, A; Silva, E O; Alonso, L. G; Brunoni, Décio ; Alonso, Nivaldo ; Richieri-Costa, Antonio ; Cavalcanti, D; Carakushansky, Gerson; Zatz, Mayana ; Passos-Bueno, Maria Rita
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidades: IB, HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SPLENDORE, A et al. Characterization of TCOF1 mutations in Brazilian patients affected with treacher Collins syndrome. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/4c7bde96-0256-41a2-93c4-556cc4d197f5/1052265.PDF. Acesso em: 21 out. 2025. , 1999
APA
Splendore, A., Silva, E. O., Alonso, L. G., Brunoni, D., Alonso, N., Richieri-Costa, A., et al. (1999). Characterization of TCOF1 mutations in Brazilian patients affected with treacher Collins syndrome. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/4c7bde96-0256-41a2-93c4-556cc4d197f5/1052265.PDF
NLM
Splendore A, Silva EO, Alonso LG, Brunoni D, Alonso N, Richieri-Costa A, Cavalcanti D, Carakushansky G, Zatz M, Passos-Bueno MR. Characterization of TCOF1 mutations in Brazilian patients affected with treacher Collins syndrome [Internet]. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/4c7bde96-0256-41a2-93c4-556cc4d197f5/1052265.PDF
Vancouver
Splendore A, Silva EO, Alonso LG, Brunoni D, Alonso N, Richieri-Costa A, Cavalcanti D, Carakushansky G, Zatz M, Passos-Bueno MR. Characterization of TCOF1 mutations in Brazilian patients affected with treacher Collins syndrome [Internet]. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ] Available from: https://repositorio.usp.br/directbitstream/4c7bde96-0256-41a2-93c4-556cc4d197f5/1052265.PDF
Trabalho de evento-resumo periodico
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations (1999)
Bernardino, A L F; Ferri, A; Passos-Bueno, Maria Rita ; Kim, C A E; Nakaie, C M A; Gomes, C. E. T.; Damasceno, N.
Fonte: American Journal of Human Genetics. Nome do evento: American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDINO, A L F et al. Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 1999
APA
Bernardino, A. L. F., Ferri, A., Passos-Bueno, M. R., Kim, C. A. E., Nakaie, C. M. A., Gomes, C. E. T., & Damasceno, N. (1999). Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.
NLM
Bernardino ALF, Ferri A, Passos-Bueno MR, Kim CAE, Nakaie CMA, Gomes CET, Damasceno N. Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]
Vancouver
Bernardino ALF, Ferri A, Passos-Bueno MR, Kim CAE, Nakaie CMA, Gomes CET, Damasceno N. Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2025 out. 21 ]

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