ReP USP - Resultado da busca

Trabalho de evento-resumo
Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family (2017)
Joaquim, T. M.; Souza, D. C. de; Grangeiro, C. H. P.; Huber, Jair; Laus, Ana Carolina; Laureano, L. A. F.; Squire, Jeremy Andrew; Martelli, Lúcia Regina
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: BIOMARCADORES, CROMOSSOMOS, GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JOAQUIM, T. M. et al. Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family. 2017, Anais.. Copenhagen: ESHG, 2017. . Acesso em: 26 out. 2025.
APA
Joaquim, T. M., Souza, D. C. de, Grangeiro, C. H. P., Huber, J., Laus, A. C., Laureano, L. A. F., et al. (2017). Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family. In Abstracts. Copenhagen: ESHG.
NLM
Joaquim TM, Souza DC de, Grangeiro CHP, Huber J, Laus AC, Laureano LAF, Squire JA, Martelli LR. Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family. Abstracts. 2017 ;[citado 2025 out. 26 ]
Vancouver
Joaquim TM, Souza DC de, Grangeiro CHP, Huber J, Laus AC, Laureano LAF, Squire JA, Martelli LR. Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family. Abstracts. 2017 ;[citado 2025 out. 26 ]
Trabalho de evento-resumo
Genome-wide copy number variation analysis in systemic lupus erythematosus (2015)
Barbosa, F. B; Simioni, M; Torres, F. R; Donadi, Eduardo Antônio; Gil-da-Silva-Lopes, V. L; Simões, Aguinaldo Luiz
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: LÚPUS ERITEMATOSO SISTÊMICO, CITOGENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, F. B et al. Genome-wide copy number variation analysis in systemic lupus erythematosus. 2015, Anais.. Glasgow: ESHG, 2015. . Acesso em: 26 out. 2025.
APA
Barbosa, F. B., Simioni, M., Torres, F. R., Donadi, E. A., Gil-da-Silva-Lopes, V. L., & Simões, A. L. (2015). Genome-wide copy number variation analysis in systemic lupus erythematosus. In Abstracts. Glasgow: ESHG.
NLM
Barbosa FB, Simioni M, Torres FR, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Genome-wide copy number variation analysis in systemic lupus erythematosus. Abstracts. 2015 ;[citado 2025 out. 26 ]
Vancouver
Barbosa FB, Simioni M, Torres FR, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Genome-wide copy number variation analysis in systemic lupus erythematosus. Abstracts. 2015 ;[citado 2025 out. 26 ]
Trabalho de evento-resumo
Recurrent copy number alterations in prostate cancer: an in silico meta-analysis of publicly available genomic data (2014)
Squire, Jeremy Andrew; Greer, P.; Williams, J.
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: FMRP
Assunto: NEOPLASIAS PROSTÁTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SQUIRE, Jeremy Andrew e GREER, P. e WILLIAMS, J. Recurrent copy number alterations in prostate cancer: an in silico meta-analysis of publicly available genomic data. 2014, Anais.. Milan: ESHG, 2014. . Acesso em: 26 out. 2025.
APA
Squire, J. A., Greer, P., & Williams, J. (2014). Recurrent copy number alterations in prostate cancer: an in silico meta-analysis of publicly available genomic data. In Abstracts. Milan: ESHG.
NLM
Squire JA, Greer P, Williams J. Recurrent copy number alterations in prostate cancer: an in silico meta-analysis of publicly available genomic data. Abstracts. 2014 ;[citado 2025 out. 26 ]
Vancouver
Squire JA, Greer P, Williams J. Recurrent copy number alterations in prostate cancer: an in silico meta-analysis of publicly available genomic data. Abstracts. 2014 ;[citado 2025 out. 26 ]
Trabalho de evento-resumo
Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding (2014)
Tavares, Vanessa Luiza; Gordon, Christhofer T.; Torres, T.; Voisin, N.; Bertola, D.; Ceide, Roseli Maria Zechi; Tan, T. Y.; Heggie, A. A. C.; Propst, E.; Papsin, B. C.; Nakata, Nancy Mizue Kokitsu; Guion-Almeida, Maria Leine; Pittoli, Siulan Vendramini Pailovich; Lyonnet, Stanislas; Amiel, Jeanne; Passos-Bueno, Maria Rita
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, MALFORMAÇÕES, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAVARES, Vanessa Luiza et al. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. 2014, Anais.. Milan: ESHG, 2014. . Acesso em: 26 out. 2025.
APA
Tavares, V. L., Gordon, C. T., Torres, T., Voisin, N., Bertola, D., Ceide, R. M. Z., et al. (2014). Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. In Abstracts. Milan: ESHG.
NLM
Tavares VL, Gordon CT, Torres T, Voisin N, Bertola D, Ceide RMZ, Tan TY, Heggie AAC, Propst E, Papsin BC, Nakata NMK, Guion-Almeida ML, Pittoli SVP, Lyonnet S, Amiel J, Passos-Bueno MR. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. Abstracts. 2014 ;[citado 2025 out. 26 ]
Vancouver
Tavares VL, Gordon CT, Torres T, Voisin N, Bertola D, Ceide RMZ, Tan TY, Heggie AAC, Propst E, Papsin BC, Nakata NMK, Guion-Almeida ML, Pittoli SVP, Lyonnet S, Amiel J, Passos-Bueno MR. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. Abstracts. 2014 ;[citado 2025 out. 26 ]
Trabalho de evento-resumo
Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears (2014)
Gordon, Christhofer T.; Petit, Florence; Kroisel, P.; Jakobsen, Linda; Ceide, Roseli Maria Zechi; Oufadem, Myriam; Bole-Feysot, C.; Nitschke, Patrick; Munnich, Arnold; Lyonnet, Stanislas; Holder-Espinasse, M.; Amiel, Jeanne
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, MALFORMAÇÕES, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GORDON, Christhofer T. et al. Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears. 2014, Anais.. Milan: ESHG, 2014. . Acesso em: 26 out. 2025.
APA
Gordon, C. T., Petit, F., Kroisel, P., Jakobsen, L., Ceide, R. M. Z., Oufadem, M., et al. (2014). Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears. In Abstracts. Milan: ESHG.
NLM
Gordon CT, Petit F, Kroisel P, Jakobsen L, Ceide RMZ, Oufadem M, Bole-Feysot C, Nitschke P, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears. Abstracts. 2014 ;[citado 2025 out. 26 ]
Vancouver
Gordon CT, Petit F, Kroisel P, Jakobsen L, Ceide RMZ, Oufadem M, Bole-Feysot C, Nitschke P, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears. Abstracts. 2014 ;[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Genotype-phenotype correlation with ring chromosome 11 (2014)
Martelli, Lucia Regina; Gomes, A. G.; Grangeiro, C. H. P.; Pereira, C. S.; Silva, L. R.; Scarparo, R. M.; Squire, Jeremy Andrew
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, CROMOSSOMOS HUMANOS 6-12
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTELLI, Lucia Regina et al. Genotype-phenotype correlation with ring chromosome 11. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2014
APA
Martelli, L. R., Gomes, A. G., Grangeiro, C. H. P., Pereira, C. S., Silva, L. R., Scarparo, R. M., & Squire, J. A. (2014). Genotype-phenotype correlation with ring chromosome 11. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Martelli LR, Gomes AG, Grangeiro CHP, Pereira CS, Silva LR, Scarparo RM, Squire JA. Genotype-phenotype correlation with ring chromosome 11. European Journal of Human Genetics. 2014 ; 22 451.[citado 2025 out. 26 ]
Vancouver
Martelli LR, Gomes AG, Grangeiro CHP, Pereira CS, Silva LR, Scarparo RM, Squire JA. Genotype-phenotype correlation with ring chromosome 11. European Journal of Human Genetics. 2014 ; 22 451.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Analysis of HOX genes in patients with laryngeal squamous cell carcinoma (2013)
Bueno, R. de Barros e Lima; Pinheiro, D. Guariz; Zanette, D. L.; Mamede, Rui Celso Martins; Silva Júnior, Wilson Araújo da
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: NEOPLASIAS DE CABEÇA E PESCOÇO, CARCINOMA DE CÉLULAS ESCAMOSAS, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BUENO, R. de Barros e Lima et al. Analysis of HOX genes in patients with laryngeal squamous cell carcinoma. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2013
APA
Bueno, R. de B. e L., Pinheiro, D. G., Zanette, D. L., Mamede, R. C. M., & Silva Júnior, W. A. da. (2013). Analysis of HOX genes in patients with laryngeal squamous cell carcinoma. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Bueno R de B e L, Pinheiro DG, Zanette DL, Mamede RCM, Silva Júnior WA da. Analysis of HOX genes in patients with laryngeal squamous cell carcinoma. European Journal of Human Genetics. 2013 ; 21 302.[citado 2025 out. 26 ]
Vancouver
Bueno R de B e L, Pinheiro DG, Zanette DL, Mamede RCM, Silva Júnior WA da. Analysis of HOX genes in patients with laryngeal squamous cell carcinoma. European Journal of Human Genetics. 2013 ; 21 302.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Altered expression of immune-related genes in children with down syndrome (2013)
Zampieri, B. L.; Biselli, J. M.; Victorino, D. B.; Silva, C. R. S.; Souza, J. E. S.; Bürger, M. C.; Silva Júnior, Wilson Araújo da; Goloni-Bertollo, E. M.; Pavarino, E. C.
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: SÍNDROME DE DOWN, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZAMPIERI, B. L. et al. Altered expression of immune-related genes in children with down syndrome. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2013
APA
Zampieri, B. L., Biselli, J. M., Victorino, D. B., Silva, C. R. S., Souza, J. E. S., Bürger, M. C., et al. (2013). Altered expression of immune-related genes in children with down syndrome. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Zampieri BL, Biselli JM, Victorino DB, Silva CRS, Souza JES, Bürger MC, Silva Júnior WA da, Goloni-Bertollo EM, Pavarino EC. Altered expression of immune-related genes in children with down syndrome. European Journal of Human Genetics. 2013 ; 21 454.[citado 2025 out. 26 ]
Vancouver
Zampieri BL, Biselli JM, Victorino DB, Silva CRS, Souza JES, Bürger MC, Silva Júnior WA da, Goloni-Bertollo EM, Pavarino EC. Altered expression of immune-related genes in children with down syndrome. European Journal of Human Genetics. 2013 ; 21 454.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Population stratification assessment and genomic control in Brazilian Head and Neck Squamous cell carcinoma (HNSCC) patients (2012)
Araújo, L. F.; Luizon, M. R.; Molfetta, G. A.; Ferreira, C. A.; Marques, A. A.; Ribeiro-Santos, A. K.; Santos, S. E.; Silva Júnior, Wilson Araújo da
Source: European Journal of Humana Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, GENÉTICA DE POPULAÇÕES, NEOPLASIAS DE CABEÇA E PESCOÇO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAÚJO, L. F. et al. Population stratification assessment and genomic control in Brazilian Head and Neck Squamous cell carcinoma (HNSCC) patients. European Journal of Humana Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2012
APA
Araújo, L. F., Luizon, M. R., Molfetta, G. A., Ferreira, C. A., Marques, A. A., Ribeiro-Santos, A. K., et al. (2012). Population stratification assessment and genomic control in Brazilian Head and Neck Squamous cell carcinoma (HNSCC) patients. European Journal of Humana Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Araújo LF, Luizon MR, Molfetta GA, Ferreira CA, Marques AA, Ribeiro-Santos AK, Santos SE, Silva Júnior WA da. Population stratification assessment and genomic control in Brazilian Head and Neck Squamous cell carcinoma (HNSCC) patients. European Journal of Humana Genetics. 2012 ; 20 162.[citado 2025 out. 26 ]
Vancouver
Araújo LF, Luizon MR, Molfetta GA, Ferreira CA, Marques AA, Ribeiro-Santos AK, Santos SE, Silva Júnior WA da. Population stratification assessment and genomic control in Brazilian Head and Neck Squamous cell carcinoma (HNSCC) patients. European Journal of Humana Genetics. 2012 ; 20 162.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Ancestry informative markers set in brazilian amerindians and ancestry estimates in brazilian quilombo remnant communities (2012)
Wiezel, C. E. V.; Luizon, M. R.; Santos, S. M. B.; Abé-Sandes, K.; Sousa, I. R.; Muniz, Y. C. N.; Mendes Júnior, Celso Teixeira; Simões, Aguinaldo Luiz
Source: European Journal of Humana Genetics. Conference titles: European Human Genetics Conference. Unidades: FFCLRP, FMRP
Subjects: GENÉTICA DE POPULAÇÕES, QUILOMBOS, ANCESTRAIS (ESTIMATIVA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WIEZEL, C. E. V. et al. Ancestry informative markers set in brazilian amerindians and ancestry estimates in brazilian quilombo remnant communities. European Journal of Humana Genetics. London: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2012
APA
Wiezel, C. E. V., Luizon, M. R., Santos, S. M. B., Abé-Sandes, K., Sousa, I. R., Muniz, Y. C. N., et al. (2012). Ancestry informative markers set in brazilian amerindians and ancestry estimates in brazilian quilombo remnant communities. European Journal of Humana Genetics. London: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo.
NLM
Wiezel CEV, Luizon MR, Santos SMB, Abé-Sandes K, Sousa IR, Muniz YCN, Mendes Júnior CT, Simões AL. Ancestry informative markers set in brazilian amerindians and ancestry estimates in brazilian quilombo remnant communities. European Journal of Humana Genetics. 2012 ; 20 162.[citado 2025 out. 26 ]
Vancouver
Wiezel CEV, Luizon MR, Santos SMB, Abé-Sandes K, Sousa IR, Muniz YCN, Mendes Júnior CT, Simões AL. Ancestry informative markers set in brazilian amerindians and ancestry estimates in brazilian quilombo remnant communities. European Journal of Humana Genetics. 2012 ; 20 162.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
BRCA1 mutation screening in brazilian hereditary breast cancer and ovary syndrome using high resolution melting (2012)
Cury, N. M.; Ferraz, Victor Evangelista de Faria; Luizon, M. R.; Ferreira, C. A.; Marques, A. A.; Silva Júnior, Wilson Araújo da
Source: European Journal of Humana Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: NEOPLASIAS MAMÁRIAS, NEOPLASIAS OVARIANAS, HEREDITARIEDADE, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CURY, N. M. et al. BRCA1 mutation screening in brazilian hereditary breast cancer and ovary syndrome using high resolution melting. European Journal of Humana Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2012
APA
Cury, N. M., Ferraz, V. E. de F., Luizon, M. R., Ferreira, C. A., Marques, A. A., & Silva Júnior, W. A. da. (2012). BRCA1 mutation screening in brazilian hereditary breast cancer and ovary syndrome using high resolution melting. European Journal of Humana Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Cury NM, Ferraz VE de F, Luizon MR, Ferreira CA, Marques AA, Silva Júnior WA da. BRCA1 mutation screening in brazilian hereditary breast cancer and ovary syndrome using high resolution melting. European Journal of Humana Genetics. 2012 ; 20 162.[citado 2025 out. 26 ]
Vancouver
Cury NM, Ferraz VE de F, Luizon MR, Ferreira CA, Marques AA, Silva Júnior WA da. BRCA1 mutation screening in brazilian hereditary breast cancer and ovary syndrome using high resolution melting. European Journal of Humana Genetics. 2012 ; 20 162.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Cytogenetics studies in mild mental retardation (2011)
Pina Neto, João Monteiro de; Abreu, L. S.; Mazzucatto, L. F.; Lourenço, C. M.; Batista, L. M.
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: RETARDO MENTAL, CARIOTIPAGEM, CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINA NETO, João Monteiro de et al. Cytogenetics studies in mild mental retardation. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2011
APA
Pina Neto, J. M. de, Abreu, L. S., Mazzucatto, L. F., Lourenço, C. M., & Batista, L. M. (2011). Cytogenetics studies in mild mental retardation. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Pina Neto JM de, Abreu LS, Mazzucatto LF, Lourenço CM, Batista LM. Cytogenetics studies in mild mental retardation. European Journal of Human Genetics. 2011 ; 19 156.[citado 2025 out. 26 ]
Vancouver
Pina Neto JM de, Abreu LS, Mazzucatto LF, Lourenço CM, Batista LM. Cytogenetics studies in mild mental retardation. European Journal of Human Genetics. 2011 ; 19 156.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Admixture dynamics in Brazilian afro-derivaded populations revealed by genetic and demographic data (2007)
Simões, Aguinaldo Luiz; Luizon, Marcelo Rizzatti; Rainha de Souza, I.; Barbosa, A. L.; Abé-Sandes, K.; Sousa, S.
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Assunto: HEREDITARIEDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIMÕES, Aguinaldo Luiz et al. Admixture dynamics in Brazilian afro-derivaded populations revealed by genetic and demographic data. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2007
APA
Simões, A. L., Luizon, M. R., Rainha de Souza, I., Barbosa, A. L., Abé-Sandes, K., & Sousa, S. (2007). Admixture dynamics in Brazilian afro-derivaded populations revealed by genetic and demographic data. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Simões AL, Luizon MR, Rainha de Souza I, Barbosa AL, Abé-Sandes K, Sousa S. Admixture dynamics in Brazilian afro-derivaded populations revealed by genetic and demographic data. European Journal of Human Genetics. 2007 ; 15 286.[citado 2025 out. 26 ]
Vancouver
Simões AL, Luizon MR, Rainha de Souza I, Barbosa AL, Abé-Sandes K, Sousa S. Admixture dynamics in Brazilian afro-derivaded populations revealed by genetic and demographic data. European Journal of Human Genetics. 2007 ; 15 286.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
A study of FGFR3 gene mutations in brazilian patients with achondroplastia, hypochondroplasia and thanatophoric dysplasia (2007)
Pina Neto, João Monteiro de; Ortolan, Daniela; Silva Júnior, Wilson Araújo da
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: POLIMORFISMO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINA NETO, João Monteiro de e ORTOLAN, Daniela e SILVA JÚNIOR, Wilson Araújo da. A study of FGFR3 gene mutations in brazilian patients with achondroplastia, hypochondroplasia and thanatophoric dysplasia. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2007
APA
Pina Neto, J. M. de, Ortolan, D., & Silva Júnior, W. A. da. (2007). A study of FGFR3 gene mutations in brazilian patients with achondroplastia, hypochondroplasia and thanatophoric dysplasia. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Pina Neto JM de, Ortolan D, Silva Júnior WA da. A study of FGFR3 gene mutations in brazilian patients with achondroplastia, hypochondroplasia and thanatophoric dysplasia. European Journal of Human Genetics. 2007 ; 15 196.[citado 2025 out. 26 ]
Vancouver
Pina Neto JM de, Ortolan D, Silva Júnior WA da. A study of FGFR3 gene mutations in brazilian patients with achondroplastia, hypochondroplasia and thanatophoric dysplasia. European Journal of Human Genetics. 2007 ; 15 196.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Hypometylation at the KvDMR in clinically normal children conceived by assisted reproductive technologies (2007)
Gomes, M. V. M.; Huber, J.; Ferriani, Rui Alberto; Ramos, Ester Silveira
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Assunto: REPRODUÇÃO (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, M. V. M. et al. Hypometylation at the KvDMR in clinically normal children conceived by assisted reproductive technologies. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2007
APA
Gomes, M. V. M., Huber, J., Ferriani, R. A., & Ramos, E. S. (2007). Hypometylation at the KvDMR in clinically normal children conceived by assisted reproductive technologies. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Gomes MVM, Huber J, Ferriani RA, Ramos ES. Hypometylation at the KvDMR in clinically normal children conceived by assisted reproductive technologies. European Journal of Human Genetics. 2007 ; 15 180.[citado 2025 out. 26 ]
Vancouver
Gomes MVM, Huber J, Ferriani RA, Ramos ES. Hypometylation at the KvDMR in clinically normal children conceived by assisted reproductive technologies. European Journal of Human Genetics. 2007 ; 15 180.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Gestational hypertensive disorders, newborn birh weigth and maternal IGF2/Apal and H19/Rsal polymorphisms (2007)
Araújo, F. M.; Soares, M. R.; Gomes, M. V. M.; Duarte, Geraldo; Marcondes, C. R.; Vozzi, P. A.; Lôbo, Raysildo Barbosa; Ramos, Ester Silveira
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: POLIMORFISMO, HIPERTENSÃO NA GRAVIDEZ
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAÚJO, F. M. et al. Gestational hypertensive disorders, newborn birh weigth and maternal IGF2/Apal and H19/Rsal polymorphisms. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2007
APA
Araújo, F. M., Soares, M. R., Gomes, M. V. M., Duarte, G., Marcondes, C. R., Vozzi, P. A., et al. (2007). Gestational hypertensive disorders, newborn birh weigth and maternal IGF2/Apal and H19/Rsal polymorphisms. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Araújo FM, Soares MR, Gomes MVM, Duarte G, Marcondes CR, Vozzi PA, Lôbo RB, Ramos ES. Gestational hypertensive disorders, newborn birh weigth and maternal IGF2/Apal and H19/Rsal polymorphisms. European Journal of Human Genetics. 2007 ; 15 251.[citado 2025 out. 26 ]
Vancouver
Araújo FM, Soares MR, Gomes MVM, Duarte G, Marcondes CR, Vozzi PA, Lôbo RB, Ramos ES. Gestational hypertensive disorders, newborn birh weigth and maternal IGF2/Apal and H19/Rsal polymorphisms. European Journal of Human Genetics. 2007 ; 15 251.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly (2007)
Ramos, Ester Silveira; Araújo, A.; Martinhago, C. D.; Martelli, Lúcia Regina; Reis, Rosana Maria dos; Melo, D. G.
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: ANORMALIDADES CROMOSSÔMICAS, SAÚDE DA MULHER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Ester Silveira et al. Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2007
APA
Ramos, E. S., Araújo, A., Martinhago, C. D., Martelli, L. R., Reis, R. M. dos, & Melo, D. G. (2007). Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Ramos ES, Araújo A, Martinhago CD, Martelli LR, Reis RM dos, Melo DG. Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly. European Journal of Human Genetics. 2007 ; 15 92.[citado 2025 out. 26 ]
Vancouver
Ramos ES, Araújo A, Martinhago CD, Martelli LR, Reis RM dos, Melo DG. Six pregnancies in a woman with Turner syndrome, including a case of holoprosencephaly. European Journal of Human Genetics. 2007 ; 15 92.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Lack of evidence of monosomy 1p36in patients with prader-will-like phenotype (2007)
Rodríguez, V. R.; Mazzucatto, Luiz Fernando; Pina Neto, João Monteiro de
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: CITOGENÉTICA, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODRÍGUEZ, V. R. e MAZZUCATTO, Luiz Fernando e PINA NETO, João Monteiro de. Lack of evidence of monosomy 1p36in patients with prader-will-like phenotype. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2007
APA
Rodríguez, V. R., Mazzucatto, L. F., & Pina Neto, J. M. de. (2007). Lack of evidence of monosomy 1p36in patients with prader-will-like phenotype. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Rodríguez VR, Mazzucatto LF, Pina Neto JM de. Lack of evidence of monosomy 1p36in patients with prader-will-like phenotype. European Journal of Human Genetics. 2007 ; 15 85.[citado 2025 out. 26 ]
Vancouver
Rodríguez VR, Mazzucatto LF, Pina Neto JM de. Lack of evidence of monosomy 1p36in patients with prader-will-like phenotype. European Journal of Human Genetics. 2007 ; 15 85.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Androgen insensitivity syndrome: mutations in exon 3 of AR gene in patients with partial and mild forms (2007)
Vretos, C.; Ramos, Ester Silveira
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: RECEPTORES ANDROGÊNICOS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VRETOS, C. e RAMOS, Ester Silveira. Androgen insensitivity syndrome: mutations in exon 3 of AR gene in patients with partial and mild forms. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2007
APA
Vretos, C., & Ramos, E. S. (2007). Androgen insensitivity syndrome: mutations in exon 3 of AR gene in patients with partial and mild forms. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Vretos C, Ramos ES. Androgen insensitivity syndrome: mutations in exon 3 of AR gene in patients with partial and mild forms. European Journal of Human Genetics. 2007 ; 15 179.[citado 2025 out. 26 ]
Vancouver
Vretos C, Ramos ES. Androgen insensitivity syndrome: mutations in exon 3 of AR gene in patients with partial and mild forms. European Journal of Human Genetics. 2007 ; 15 179.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Partially isolated communities founded by Azoreans in the Santa Catarina Island, Southern Brazil (2007)
Muniz, Y. C. N.; Muniz, Y. C. N.; Souza, I. R; Simões, Aguinaldo Luiz
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Assunto: HEREDITARIEDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MUNIZ, Y. C. N. et al. Partially isolated communities founded by Azoreans in the Santa Catarina Island, Southern Brazil. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2007
APA
Muniz, Y. C. N., Muniz, Y. C. N., Souza, I. R., & Simões, A. L. (2007). Partially isolated communities founded by Azoreans in the Santa Catarina Island, Southern Brazil. European Journal of Human Genetics. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Muniz YCN, Muniz YCN, Souza IR, Simões AL. Partially isolated communities founded by Azoreans in the Santa Catarina Island, Southern Brazil. European Journal of Human Genetics. 2007 ; 15 284.[citado 2025 out. 26 ]
Vancouver
Muniz YCN, Muniz YCN, Souza IR, Simões AL. Partially isolated communities founded by Azoreans in the Santa Catarina Island, Southern Brazil. European Journal of Human Genetics. 2007 ; 15 284.[citado 2025 out. 26 ]

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Date published

Subjects