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Artigo de periodico-carta/editorial
Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] (1999)
Gaspar, D A; Pavanello, R.C; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Andre, M; Steman, S; Wyszynski, D. F; Matioli, Sergio Russo
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, LÁBIO FISSURADO, MUTAÇÃO GENÉTICA, POLIMORFISMO, MALFORMAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GASPAR, D A et al. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta]. American Journal of Medical Genetics. Hoboken: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M. Acesso em: 18 abr. 2024. , 1999
APA
Gaspar, D. A., Pavanello, R. C., Zatz, M., Passos-Bueno, M. R., Andre, M., Steman, S., et al. (1999). Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta]. American Journal of Medical Genetics. Hoboken: Instituto de Biociências, Universidade de São Paulo. doi:10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.
NLM
Gaspar DA, Pavanello RC, Zatz M, Passos-Bueno MR, Andre M, Steman S, Wyszynski DF, Matioli SR. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] [Internet]. American Journal of Medical Genetics. 1999 ; 87 197-199.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M
Vancouver
Gaspar DA, Pavanello RC, Zatz M, Passos-Bueno MR, Andre M, Steman S, Wyszynski DF, Matioli SR. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] [Internet]. American Journal of Medical Genetics. 1999 ; 87 197-199.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M
Artigo de periodico
DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population (1999)
Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Costa, Sílvia S; Angeli, Claudia Blanes
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia et al. DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population. American Journal of Medical Genetics, v. 84, n. 3, p. 204-207, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C204::aid-ajmg7%3E3.0.co;2-j. Acesso em: 18 abr. 2024.
APA
Mingroni Netto, R. C., Vianna-Morgante, A. M., Costa, S. S., & Angeli, C. B. (1999). DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population. American Journal of Medical Genetics, 84( 3), 204-207. doi:10.1002/(sici)1096-8628(19990528)84:3%3C204::aid-ajmg7%3E3.0.co;2-j
NLM
Mingroni Netto RC, Vianna-Morgante AM, Costa SS, Angeli CB. DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population [Internet]. American Journal of Medical Genetics. 1999 ;84( 3): 204-207.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C204::aid-ajmg7%3E3.0.co;2-j
Vancouver
Mingroni Netto RC, Vianna-Morgante AM, Costa SS, Angeli CB. DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population [Internet]. American Journal of Medical Genetics. 1999 ;84( 3): 204-207.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C204::aid-ajmg7%3E3.0.co;2-j
Artigo de periodico
Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys (1999)
Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Aguiar, Marcos J B; Costa, Sílvia S; Pena, Sérgio D J
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HADDAD, Luciana Amaral et al. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys. American Journal of Medical Genetics, v. 84, n. 3, p. 198-201, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w. Acesso em: 18 abr. 2024.
APA
Haddad, L. A., Mingroni Netto, R. C., Vianna-Morgante, A. M., Aguiar, M. J. B., Costa, S. S., & Pena, S. D. J. (1999). Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys. American Journal of Medical Genetics, 84( 3), 198-201. doi:10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
NLM
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Aguiar MJB, Costa SS, Pena SDJ. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys [Internet]. American Journal of Medical Genetics. 1999 ; 84( 3): 198-201.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
Vancouver
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Aguiar MJB, Costa SS, Pena SDJ. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys [Internet]. American Journal of Medical Genetics. 1999 ; 84( 3): 198-201.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
Artigo de periodico-carta/editorial
Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta] (1999)
Pereira, Lygia da Veiga ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Lygia da Veiga e ZATZ, Mayana. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 18 abr. 2024. , 1999
APA
Pereira, L. da V., & Zatz, M. (1999). Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Pereira L da V, Zatz M. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. 1999 ; 87 86-87.[citado 2024 abr. 18 ]
Vancouver
Pereira L da V, Zatz M. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. 1999 ; 87 86-87.[citado 2024 abr. 18 ]
Artigo de periodico
Genetic counseling for childless women at risk for Duchenne muscular dystrophy (1999)
Eggers, Sabine; Pavanello, Rita de Cássia M.; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EGGERS, Sabine et al. Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, v. 86, p. 447-453, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p. Acesso em: 18 abr. 2024.
APA
Eggers, S., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (1999). Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, 86, 447-453. doi:10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
NLM
Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
Vancouver
Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
Artigo de periodico
Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G (1999)
Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, Eloisa S.; Zatz, Mayana
Source: American Journal of Medical 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. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics, v. 82, p. 392-398, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0. Acesso em: 18 abr. 2024.
APA
Passos-Bueno, M. R., Vainzof, M., Moreira, E. S., & Zatz, M. (1999). Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics, 82, 392-398. doi:10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
NLM
Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G [Internet]. American Journal of Medical Genetics. 1999 ; 82 392-398.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
Vancouver
Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G [Internet]. American Journal of Medical Genetics. 1999 ; 82 392-398.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
Artigo de periodico-carta/editorial
Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial] (1999)
Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIANNA-MORGANTE, Angela M. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 18 abr. 2024. , 1999
APA
Vianna-Morgante, A. M. (1999). Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Vianna-Morgante AM. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. 1999 ; 83( 4): 326.[citado 2024 abr. 18 ]
Vancouver
Vianna-Morgante AM. Twinning and premature ovarian failure in premutation fragile X carriers. [Carta/Editorial]. American Journal of Medical Genetics. 1999 ; 83( 4): 326.[citado 2024 abr. 18 ]
Artigo de periodico
Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data (1999)
Allingham-Hawkins, Diane J; Babul-Hirji, Riyana; Chitayat, David; Holden, Jeanette J A; Yang, Kathy T; Lee, C; Hudson, R; Gorwill, H; Nolin, Sarah L; Glicksman, Anne; Jenkins, Edmund C; Brown, W Ted; Howard-Peebles, Patricia N; Becchi, Cindy; Cummings, Emilie; Fallon, Lee; Seitz, Suzanne; Black, Susan H; Vianna-Morgante, Angela M ; Costa, Silvia S; Otto, Paulo A ; Mingroni Netto, Regina Celia ; Murray, Anna; Webb, J; MacSwinney, F; Dennis, N; Jacobs, Patricia A; Syrrou, Maria; Georgiou, Ioannis; Patsalis, Phillipos C; Uzielli, Maria L Giovannucci; Guarducci, S; Lapi, E; Cecconi, A; Ricci, U; Ricotti, G; Biondi, C; Scarselli, B; Vieri, F
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALLINGHAM-HAWKINS, Diane J et al. Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data. American Journal of Medical Genetics, v. 83. n. 4, p. 322-325, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b. Acesso em: 18 abr. 2024.
APA
Allingham-Hawkins, D. J., Babul-Hirji, R., Chitayat, D., Holden, J. J. A., Yang, K. T., Lee, C., et al. (1999). Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data. American Journal of Medical Genetics, 83. n. 4, 322-325. doi:10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b
NLM
Allingham-Hawkins DJ, Babul-Hirji R, Chitayat D, Holden JJA, Yang KT, Lee C, Hudson R, Gorwill H, Nolin SL, Glicksman A, Jenkins EC, Brown WT, Howard-Peebles PN, Becchi C, Cummings E, Fallon L, Seitz S, Black SH, Vianna-Morgante AM, Costa SS, Otto PA, Mingroni Netto RC, Murray A, Webb J, MacSwinney F, Dennis N, Jacobs PA, Syrrou M, Georgiou I, Patsalis PC, Uzielli MLG, Guarducci S, Lapi E, Cecconi A, Ricci U, Ricotti G, Biondi C, Scarselli B, Vieri F. Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data [Internet]. American Journal of Medical Genetics. 1999 ; 83. n. 4 322-325.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b
Vancouver
Allingham-Hawkins DJ, Babul-Hirji R, Chitayat D, Holden JJA, Yang KT, Lee C, Hudson R, Gorwill H, Nolin SL, Glicksman A, Jenkins EC, Brown WT, Howard-Peebles PN, Becchi C, Cummings E, Fallon L, Seitz S, Black SH, Vianna-Morgante AM, Costa SS, Otto PA, Mingroni Netto RC, Murray A, Webb J, MacSwinney F, Dennis N, Jacobs PA, Syrrou M, Georgiou I, Patsalis PC, Uzielli MLG, Guarducci S, Lapi E, Cecconi A, Ricci U, Ricotti G, Biondi C, Scarselli B, Vieri F. Fragile X premutation is a significant risk factor for premature ovarian failure: the international collaborative POF in fragile X study - preliminary data [Internet]. American Journal of Medical Genetics. 1999 ; 83. n. 4 322-325.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990402)83:4%3C322::aid-ajmg17%3E3.0.co;2-b
Artigo de periodico
Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses (1998)
Passos-Bueno, Maria Rita ; Sertié, Andréa L; Richieri-Costa, Antonio; Alonso, Luís G; Zatz, Mayana ; Alonso, Nivaldo; Brunoni, Decio; Ribeiro, Sandra F M
Source: American Journal of Medical Genetics. Unidades: IB, HRAC
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. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics, v. 78, p. 237-241, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m. Acesso em: 18 abr. 2024.
APA
Passos-Bueno, M. R., Sertié, A. L., Richieri-Costa, A., Alonso, L. G., Zatz, M., Alonso, N., et al. (1998). Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics, 78, 237-241. doi:10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m
NLM
Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SFM. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses [Internet]. American Journal of Medical Genetics. 1998 ; 78 237-241.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m
Vancouver
Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SFM. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses [Internet]. American Journal of Medical Genetics. 1998 ; 78 237-241.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m
Artigo de periodico
Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in brazilian patients affected by bipolar disorder and schizophrenia (1998)
Oliveira, João R. Mendes de; Otto, Paulo A ; Vallada, Homero; Lauriano, Valeria; Elkis, Hélio; Lafer, Beny; Vasquez, Luciana; Gentil, Valentim; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidades: IB, FM
Subjects: BIOLOGIA, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, João R. Mendes de et al. Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in brazilian patients affected by bipolar disorder and schizophrenia. American Journal of Medical Genetics, v. 81, p. 225-227, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980508)81:3%3C225::aid-ajmg4%3E3.0.co;2-v. Acesso em: 18 abr. 2024.
APA
Oliveira, J. R. M. de, Otto, P. A., Vallada, H., Lauriano, V., Elkis, H., Lafer, B., et al. (1998). Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in brazilian patients affected by bipolar disorder and schizophrenia. American Journal of Medical Genetics, 81, 225-227. doi:10.1002/(sici)1096-8628(19980508)81:3%3C225::aid-ajmg4%3E3.0.co;2-v
NLM
Oliveira JRM de, Otto PA, Vallada H, Lauriano V, Elkis H, Lafer B, Vasquez L, Gentil V, Passos-Bueno MR, Zatz M. Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in brazilian patients affected by bipolar disorder and schizophrenia [Internet]. American Journal of Medical Genetics. 1998 ; 81 225-227.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980508)81:3%3C225::aid-ajmg4%3E3.0.co;2-v
Vancouver
Oliveira JRM de, Otto PA, Vallada H, Lauriano V, Elkis H, Lafer B, Vasquez L, Gentil V, Passos-Bueno MR, Zatz M. Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in brazilian patients affected by bipolar disorder and schizophrenia [Internet]. American Journal of Medical Genetics. 1998 ; 81 225-227.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980508)81:3%3C225::aid-ajmg4%3E3.0.co;2-v
Artigo de periodico
Social adjustment in adult males affected with progressive muscular dystrophy (1998)
Eggers, Sabine; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EGGERS, Sabine e ZATZ, Mayana. Social adjustment in adult males affected with progressive muscular dystrophy. American Journal of Medical Genetics, v. 81, p. 4-12, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980207)81:1%3C4::aid-ajmg2%3E3.0.co;2-#. Acesso em: 18 abr. 2024.
APA
Eggers, S., & Zatz, M. (1998). Social adjustment in adult males affected with progressive muscular dystrophy. American Journal of Medical Genetics, 81, 4-12. doi:10.1002/(sici)1096-8628(19980207)81:1%3C4::aid-ajmg2%3E3.0.co;2-#
NLM
Eggers S, Zatz M. Social adjustment in adult males affected with progressive muscular dystrophy [Internet]. American Journal of Medical Genetics. 1998 ; 81 4-12.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980207)81:1%3C4::aid-ajmg2%3E3.0.co;2-#
Vancouver
Eggers S, Zatz M. Social adjustment in adult males affected with progressive muscular dystrophy [Internet]. American Journal of Medical Genetics. 1998 ; 81 4-12.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980207)81:1%3C4::aid-ajmg2%3E3.0.co;2-#
Artigo de periodico
Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families (1998)
Iughetti, Paula; Otto, Paulo A ; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Marie, Suely Kazue Nagahashi
Source: American Journal of Medical Genetics. Unidades: IB, FM
Assunto: DOENÇAS DEGENERATIVAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
IUGHETTI, Paula et al. Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families. American Journal of Medical Genetics, v. 77, n. 3, p. 246-248, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980518)77:3%3C246::aid-ajmg11%3E3.3.co;2-t. Acesso em: 18 abr. 2024.
APA
Iughetti, P., Otto, P. A., Zatz, M., Passos-Bueno, M. R., & Marie, S. K. N. (1998). Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families. American Journal of Medical Genetics, 77( 3), 246-248. doi:10.1002/(sici)1096-8628(19980518)77:3%3C246::aid-ajmg11%3E3.3.co;2-t
NLM
Iughetti P, Otto PA, Zatz M, Passos-Bueno MR, Marie SKN. Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families [Internet]. American Journal of Medical Genetics. 1998 ; 77( 3): 246-248.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980518)77:3%3C246::aid-ajmg11%3E3.3.co;2-t
Vancouver
Iughetti P, Otto PA, Zatz M, Passos-Bueno MR, Marie SKN. Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families [Internet]. American Journal of Medical Genetics. 1998 ; 77( 3): 246-248.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980518)77:3%3C246::aid-ajmg11%3E3.3.co;2-t
Artigo de periodico
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases (1998)
Zatz, Mayana ; Sumita, Denilce; Campiotto, Simone; Canovas, Marta; Cerqueira, Antonia; Vainzof, Mariz ; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases. American Journal of Medical Genetics, v. 78, p. 361-365, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g. Acesso em: 18 abr. 2024.
APA
Zatz, M., Sumita, D., Campiotto, S., Canovas, M., Cerqueira, A., Vainzof, M., & Passos-Bueno, M. R. (1998). Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases. American Journal of Medical Genetics, 78, 361-365. doi:10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g
NLM
Zatz M, Sumita D, Campiotto S, Canovas M, Cerqueira A, Vainzof M, Passos-Bueno MR. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases [Internet]. American Journal of Medical Genetics. 1998 ; 78 361-365.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g
Vancouver
Zatz M, Sumita D, Campiotto S, Canovas M, Cerqueira A, Vainzof M, Passos-Bueno MR. Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases [Internet]. American Journal of Medical Genetics. 1998 ; 78 361-365.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980724)78:4%3C361::aid-ajmg11%3E3.0.co;2-g
Artigo de periodico
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers (1998)
Sumita, Denilce Ritsuko; Vainzof, Mariz ; Campiotto, Simone; Cerqueira, Antonia M; Canovas, Marta; Otto, Paulo A ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SUMITA, Denilce Ritsuko et al. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers. American Journal of Medical Genetics, v. 80, p. 356-361, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19981204)80:4%3C356::aid-ajmg10%3E3.3.co;2-f. Acesso em: 18 abr. 2024.
APA
Sumita, D. R., Vainzof, M., Campiotto, S., Cerqueira, A. M., Canovas, M., Otto, P. A., et al. (1998). Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers. American Journal of Medical Genetics, 80, 356-361. doi:10.1002/(sici)1096-8628(19981204)80:4%3C356::aid-ajmg10%3E3.3.co;2-f
NLM
Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Canovas M, Otto PA, Passos-Bueno MR, Zatz M. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers [Internet]. American Journal of Medical Genetics. 1998 ; 80 356-361.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19981204)80:4%3C356::aid-ajmg10%3E3.3.co;2-f
Vancouver
Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Canovas M, Otto PA, Passos-Bueno MR, Zatz M. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers [Internet]. American Journal of Medical Genetics. 1998 ; 80 356-361.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19981204)80:4%3C356::aid-ajmg10%3E3.3.co;2-f
Artigo de periodico
Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis (1998)
Rabbi-Bortolini, Eliete; Bernardino, Andréa L F; Lopes, Adoris L; Ferri, Adriana da Silva; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RABBI-BORTOLINI, Eliete et al. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis. American Journal of Medical Genetics, v. 76, p. 288-290, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q. Acesso em: 18 abr. 2024.
APA
Rabbi-Bortolini, E., Bernardino, A. L. F., Lopes, A. L., Ferri, A. da S., Passos-Bueno, M. R., & Zatz, M. (1998). Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis. American Journal of Medical Genetics, 76, 288-290. doi:10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
NLM
Rabbi-Bortolini E, Bernardino ALF, Lopes AL, Ferri A da S, Passos-Bueno MR, Zatz M. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis [Internet]. American Journal of Medical Genetics. 1998 ; 76 288-290.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
Vancouver
Rabbi-Bortolini E, Bernardino ALF, Lopes AL, Ferri A da S, Passos-Bueno MR, Zatz M. Sweat electrolyte and cystic fribrosis mutation analysis allows early diagnosis in brazilian children with clinical signs compatible with cystic fibrosis [Internet]. American Journal of Medical Genetics. 1998 ; 76 288-290.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980401)76:4%3C288::aid-ajmg2%3E3.3.co;2-q
Artigo de periodico
Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? (1997)
Passos-Bueno, Maria Rita ; Sertié, Andréa Laurato; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidades: IB, HRAC
Subjects: SÍNDROMES OROFACIODIGITAIS, MUTAÇÃO, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita e SERTIÉ, Andréa Laurato e RICHIERI-COSTA, Antonio. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?. American Journal of Medical Genetics, v. 71, n. 2, p. 243-245, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d. Acesso em: 18 abr. 2024.
APA
Passos-Bueno, M. R., Sertié, A. L., & Richieri-Costa, A. (1997). Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? American Journal of Medical Genetics, 71( 2), 243-245. doi:10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
NLM
Passos-Bueno MR, Sertié AL, Richieri-Costa A. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 243-245.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
Vancouver
Passos-Bueno MR, Sertié AL, Richieri-Costa A. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 243-245.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
Artigo de periodico
Fraxa premutation associated with premature ovarian failure (1996)
Vianna-Morgante, Angela M ; Costa, S. S.; Pares, A S; Verreschi, I T N
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIANNA-MORGANTE, Angela M et al. Fraxa premutation associated with premature ovarian failure. American Journal of Medical Genetics, v. 64, n. 2 , p. 373-5, 1996Tradução . . Acesso em: 18 abr. 2024.
APA
Vianna-Morgante, A. M., Costa, S. S., Pares, A. S., & Verreschi, I. T. N. (1996). Fraxa premutation associated with premature ovarian failure. American Journal of Medical Genetics, 64( 2 ), 373-5.
NLM
Vianna-Morgante AM, Costa SS, Pares AS, Verreschi ITN. Fraxa premutation associated with premature ovarian failure. American Journal of Medical Genetics. 1996 ;64( 2 ): 373-5.[citado 2024 abr. 18 ]
Vancouver
Vianna-Morgante AM, Costa SS, Pares AS, Verreschi ITN. Fraxa premutation associated with premature ovarian failure. American Journal of Medical Genetics. 1996 ;64( 2 ): 373-5.[citado 2024 abr. 18 ]
Artigo de periodico
Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism (1996)
Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral ; Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia e HADDAD, Luciana Amaral e VIANNA-MORGANTE, Angela M. Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. American Journal of Medical Genetics, v. 64, n. 2 , p. 270-3, 1996Tradução . . Acesso em: 18 abr. 2024.
APA
Mingroni Netto, R. C., Haddad, L. A., & Vianna-Morgante, A. M. (1996). Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. American Journal of Medical Genetics, 64( 2 ), 270-3.
NLM
Mingroni Netto RC, Haddad LA, Vianna-Morgante AM. Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. American Journal of Medical Genetics. 1996 ;64( 2 ): 270-3.[citado 2024 abr. 18 ]
Vancouver
Mingroni Netto RC, Haddad LA, Vianna-Morgante AM. Number of cgg repeats of the fmr1 locus in premutated and fully mutated heterozygotes and their offspring: implications for the origin of mosaicism. American Journal of Medical Genetics. 1996 ;64( 2 ): 270-3.[citado 2024 abr. 18 ]
Artigo de periodico
Encomium: Oswaldo Frota-Pessoa (1996)
Vianna-Morgante, Angela M ; Azevedo, Eliane S; Otto, Paulo A ; Opitz, John M.
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: BIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIANNA-MORGANTE, Angela M et al. Encomium: Oswaldo Frota-Pessoa. American Journal of Medical Genetics, 1996Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19960628)63:4%3C581::aid-ajmg12%3E3.0.co;2-e. Acesso em: 18 abr. 2024.
APA
Vianna-Morgante, A. M., Azevedo, E. S., Otto, P. A., & Opitz, J. M. (1996). Encomium: Oswaldo Frota-Pessoa. American Journal of Medical Genetics. doi:10.1002/(sici)1096-8628(19960628)63:4%3C581::aid-ajmg12%3E3.0.co;2-e
NLM
Vianna-Morgante AM, Azevedo ES, Otto PA, Opitz JM. Encomium: Oswaldo Frota-Pessoa [Internet]. American Journal of Medical Genetics. 1996 ;[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960628)63:4%3C581::aid-ajmg12%3E3.0.co;2-e
Vancouver
Vianna-Morgante AM, Azevedo ES, Otto PA, Opitz JM. Encomium: Oswaldo Frota-Pessoa [Internet]. American Journal of Medical Genetics. 1996 ;[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19960628)63:4%3C581::aid-ajmg12%3E3.0.co;2-e
Artigo de periodico
Identification of a supernumerary marker derived from chromosome 17 using fish (1995)
Rosenberg, Carla ; Borovik, C L; Canonaco, R S; Sichero, L C; Queiroz, A P S; Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROSENBERG, Carla et al. Identification of a supernumerary marker derived from chromosome 17 using fish. American Journal of Medical Genetics, v. 59, p. 33-5, 1995Tradução . . Acesso em: 18 abr. 2024.
APA
Rosenberg, C., Borovik, C. L., Canonaco, R. S., Sichero, L. C., Queiroz, A. P. S., & Vianna-Morgante, A. M. (1995). Identification of a supernumerary marker derived from chromosome 17 using fish. American Journal of Medical Genetics, 59, 33-5.
NLM
Rosenberg C, Borovik CL, Canonaco RS, Sichero LC, Queiroz APS, Vianna-Morgante AM. Identification of a supernumerary marker derived from chromosome 17 using fish. American Journal of Medical Genetics. 1995 ;59 33-5.[citado 2024 abr. 18 ]
Vancouver
Rosenberg C, Borovik CL, Canonaco RS, Sichero LC, Queiroz APS, Vianna-Morgante AM. Identification of a supernumerary marker derived from chromosome 17 using fish. American Journal of Medical Genetics. 1995 ;59 33-5.[citado 2024 abr. 18 ]

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