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Trabalho de evento-resumo
HLA-G gene associated with vitiligo in a Brazilian population sample (2019)
Oliveira, Maria Luiza Guimarães de ; Castelli, Luciana Caricati Veiga ; Pereira, Alison Luis Eburneo; Debortoli, Guilherme ; Marcorin, Letícia ; Fracasso, Nádia Carolina de Aguiar; Silva, Guilherme do Valle ; Souza, A. S.; Massaro, Juliana Doblas ; Simões, Aguinaldo Luiz ; Sabbagh, A.; Cardili, Renata Nahas; Donadi, Eduardo Antônio ; Castelli, E. C.; Mendes Júnior, Celso Teixeira
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Subjects: GENES, VITILIGO, DOENÇAS AUTOIMUNES, POPULAÇÃO
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ABNT
OLIVEIRA, Maria Luiza Guimarães de et al. HLA-G gene associated with vitiligo in a Brazilian population sample. 2019, Anais.. Houston: ASHG, 2019. Disponível em: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf. Acesso em: 03 jun. 2024.
APA
Oliveira, M. L. G. de, Castelli, L. C. V., Pereira, A. L. E., Debortoli, G., Marcorin, L., Fracasso, N. C. de A., et al. (2019). HLA-G gene associated with vitiligo in a Brazilian population sample. In Abstracts. Houston: ASHG. Recuperado de https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
NLM
Oliveira MLG de, Castelli LCV, Pereira ALE, Debortoli G, Marcorin L, Fracasso NC de A, Silva G do V, Souza AS, Massaro JD, Simões AL, Sabbagh A, Cardili RN, Donadi EA, Castelli EC, Mendes Júnior CT. HLA-G gene associated with vitiligo in a Brazilian population sample [Internet]. Abstracts. 2019 ;[citado 2024 jun. 03 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Vancouver
Oliveira MLG de, Castelli LCV, Pereira ALE, Debortoli G, Marcorin L, Fracasso NC de A, Silva G do V, Souza AS, Massaro JD, Simões AL, Sabbagh A, Cardili RN, Donadi EA, Castelli EC, Mendes Júnior CT. HLA-G gene associated with vitiligo in a Brazilian population sample [Internet]. Abstracts. 2019 ;[citado 2024 jun. 03 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Trabalho de evento-resumo
Prediction of eye and hair pigmentation phenotypes using the HlrisPlex system in a Brazilian admized population sample (2018)
Mendes Júnior, Celso Teixeira; Carratto, T. M. T.; Souza, F. D. N.; Marcorin, L.; Silva, G. V.; Pereira, A. L. E.; Fracasso, N. C. A.; Oliveira, M. L. G.; Debortoli, G.; Donadi, Eduardo Antônio; Simões, Aguinaldo Luiz; Castelli, Erick da Cruz
Source: Posters Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Subjects: FENÓTIPOS, PIGMENTOS, OLHO, CABELO
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ABNT
MENDES JÚNIOR, Celso Teixeira et al. Prediction of eye and hair pigmentation phenotypes using the HlrisPlex system in a Brazilian admized population sample. 2018, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2018. . Acesso em: 03 jun. 2024.
APA
Mendes Júnior, C. T., Carratto, T. M. T., Souza, F. D. N., Marcorin, L., Silva, G. V., Pereira, A. L. E., et al. (2018). Prediction of eye and hair pigmentation phenotypes using the HlrisPlex system in a Brazilian admized population sample. In Posters Abstracts. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Mendes Júnior CT, Carratto TMT, Souza FDN, Marcorin L, Silva GV, Pereira ALE, Fracasso NCA, Oliveira MLG, Debortoli G, Donadi EA, Simões AL, Castelli E da C. Prediction of eye and hair pigmentation phenotypes using the HlrisPlex system in a Brazilian admized population sample. Posters Abstracts. 2018 ;[citado 2024 jun. 03 ]
Vancouver
Mendes Júnior CT, Carratto TMT, Souza FDN, Marcorin L, Silva GV, Pereira ALE, Fracasso NCA, Oliveira MLG, Debortoli G, Donadi EA, Simões AL, Castelli E da C. Prediction of eye and hair pigmentation phenotypes using the HlrisPlex system in a Brazilian admized population sample. Posters Abstracts. 2018 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Genetics of cortical dysplasias and epilepsy treated surgically (2018)
Garcia, C. A. B.; Machado, Hélio Rubens; Silva Júnior, Wilson Araújo da; Teixeira, T. L.; Volpon, M. S.; Bali, L. L.; James, K. N.; Gleeson, J. J.
Source: Posters Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: CÓRTEX CEREBRAL, EPILEPSIA, CIRURGIA
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ABNT
GARCIA, C. A. B. et al. Genetics of cortical dysplasias and epilepsy treated surgically. 2018, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2018. . Acesso em: 03 jun. 2024.
APA
Garcia, C. A. B., Machado, H. R., Silva Júnior, W. A. da, Teixeira, T. L., Volpon, M. S., Bali, L. L., et al. (2018). Genetics of cortical dysplasias and epilepsy treated surgically. In Posters Abstracts. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Garcia CAB, Machado HR, Silva Júnior WA da, Teixeira TL, Volpon MS, Bali LL, James KN, Gleeson JJ. Genetics of cortical dysplasias and epilepsy treated surgically. Posters Abstracts. 2018 ;[citado 2024 jun. 03 ]
Vancouver
Garcia CAB, Machado HR, Silva Júnior WA da, Teixeira TL, Volpon MS, Bali LL, James KN, Gleeson JJ. Genetics of cortical dysplasias and epilepsy treated surgically. Posters Abstracts. 2018 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
LILRB1//LT2 polymorphisms detected in Brazil reveal a conserved locus with polymorphism frequencies influenced by ancestry (2018)
Castelli, Erick da Cruz; Oliveira, M. L. G.; Paz, M. A.; Souza, A. S.; Veiga-Castelli, L. C.; Marcorin, L.; Debortoli, G.; Pereira, A. L. E.; Fracasso, N. C. A.; Silva, G. V.; Simões, Aguinaldo Luiz; Sabbagh, A.; Donadi, Eduardo Antônio; Mendes Júnior, Celso Teixeira
Source: Posters Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Subjects: POLIMORFISMO, DNA
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ABNT
CASTELLI, Erick da Cruz et al. LILRB1//LT2 polymorphisms detected in Brazil reveal a conserved locus with polymorphism frequencies influenced by ancestry. 2018, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2018. . Acesso em: 03 jun. 2024.
APA
Castelli, E. da C., Oliveira, M. L. G., Paz, M. A., Souza, A. S., Veiga-Castelli, L. C., Marcorin, L., et al. (2018). LILRB1//LT2 polymorphisms detected in Brazil reveal a conserved locus with polymorphism frequencies influenced by ancestry. In Posters Abstracts. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Castelli E da C, Oliveira MLG, Paz MA, Souza AS, Veiga-Castelli LC, Marcorin L, Debortoli G, Pereira ALE, Fracasso NCA, Silva GV, Simões AL, Sabbagh A, Donadi EA, Mendes Júnior CT. LILRB1//LT2 polymorphisms detected in Brazil reveal a conserved locus with polymorphism frequencies influenced by ancestry. Posters Abstracts. 2018 ;[citado 2024 jun. 03 ]
Vancouver
Castelli E da C, Oliveira MLG, Paz MA, Souza AS, Veiga-Castelli LC, Marcorin L, Debortoli G, Pereira ALE, Fracasso NCA, Silva GV, Simões AL, Sabbagh A, Donadi EA, Mendes Júnior CT. LILRB1//LT2 polymorphisms detected in Brazil reveal a conserved locus with polymorphism frequencies influenced by ancestry. Posters Abstracts. 2018 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? (2017)
Molfetta, Greice Andreotti de; Piram, A.; Machry, A. J.; Anjos, T. O.; Marques, A. A.; Silva Júnior, Wilson Araújo da
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: OSTEOGÊNESE IMPERFEITA, GENÉTICA MÉDICA
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ABNT
MOLFETTA, Greice Andreotti de et al. Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? 2017, Anais.. Orlando: ASHG, 2017. . Acesso em: 03 jun. 2024.
APA
Molfetta, G. A. de, Piram, A., Machry, A. J., Anjos, T. O., Marques, A. A., & Silva Júnior, W. A. da. (2017). Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? In Abstracts. Orlando: ASHG.
NLM
Molfetta GA de, Piram A, Machry AJ, Anjos TO, Marques AA, Silva Júnior WA da. Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? Abstracts. 2017 ;[citado 2024 jun. 03 ]
Vancouver
Molfetta GA de, Piram A, Machry AJ, Anjos TO, Marques AA, Silva Júnior WA da. Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? Abstracts. 2017 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Molecular characterization of Brazilian patients with hereditary breast and ovarian cancer syndrome: what can we find beyond BRCA1 and BRCA2 genes ? (2017)
Carvalho, S. C. S.; Brotto, D. B.; Torrieri, Rafaella Tonani; Teixeira, L. A.; Araújo, L. F.; Plaça, J. R.; Peronni, K. C.; Silva Júnior, Wilson Araújo da
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FORP
Subjects: NEOPLASIAS MAMÁRIAS, NEOPLASIAS OVARIANAS, MUTAÇÃO GENÉTICA
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ABNT
CARVALHO, S. C. S. et al. Molecular characterization of Brazilian patients with hereditary breast and ovarian cancer syndrome: what can we find beyond BRCA1 and BRCA2 genes ? 2017, Anais.. Orlando: ASHG, 2017. . Acesso em: 03 jun. 2024.
APA
Carvalho, S. C. S., Brotto, D. B., Torrieri, R. T., Teixeira, L. A., Araújo, L. F., Plaça, J. R., et al. (2017). Molecular characterization of Brazilian patients with hereditary breast and ovarian cancer syndrome: what can we find beyond BRCA1 and BRCA2 genes ? In Abstracts. Orlando: ASHG.
NLM
Carvalho SCS, Brotto DB, Torrieri RT, Teixeira LA, Araújo LF, Plaça JR, Peronni KC, Silva Júnior WA da. Molecular characterization of Brazilian patients with hereditary breast and ovarian cancer syndrome: what can we find beyond BRCA1 and BRCA2 genes ? Abstracts. 2017 ;[citado 2024 jun. 03 ]
Vancouver
Carvalho SCS, Brotto DB, Torrieri RT, Teixeira LA, Araújo LF, Plaça JR, Peronni KC, Silva Júnior WA da. Molecular characterization of Brazilian patients with hereditary breast and ovarian cancer syndrome: what can we find beyond BRCA1 and BRCA2 genes ? Abstracts. 2017 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil (2017)
Mendes Júnior, Celso Teixeira; Pereira, A. L. E.; Marcorin, L.; Oliveira, M. L. G.; Fracasso, N. C. A.; Debortoli, G.; Silva, G. V.; Massaro, J. D.; Simões, Aguinaldo Luiz; Donadi, Eduardo Antônio; Castelli, Erick da Cruz
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Subjects: DIVERSIDADE GENÉTICA, MELANINAS, POPULAÇÃO
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ABNT
MENDES JÚNIOR, Celso Teixeira et al. MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil. 2017, Anais.. Orlando: ASHG, 2017. . Acesso em: 03 jun. 2024.
APA
Mendes Júnior, C. T., Pereira, A. L. E., Marcorin, L., Oliveira, M. L. G., Fracasso, N. C. A., Debortoli, G., et al. (2017). MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil. In Abstracts. Orlando: ASHG.
NLM
Mendes Júnior CT, Pereira ALE, Marcorin L, Oliveira MLG, Fracasso NCA, Debortoli G, Silva GV, Massaro JD, Simões AL, Donadi EA, Castelli E da C. MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil. Abstracts. 2017 ;[citado 2024 jun. 03 ]
Vancouver
Mendes Júnior CT, Pereira ALE, Marcorin L, Oliveira MLG, Fracasso NCA, Debortoli G, Silva GV, Massaro JD, Simões AL, Donadi EA, Castelli E da C. MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil. Abstracts. 2017 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
MiR-450a and miR-450b-5p negatively impact the tumorigenic potential of ovarian epithelial cancer cells (2017)
Muys, B. R.; Sousa, J. F.; Araújo, L. F.; Turaça, F.; Rodrigues, I. S.; Vidal, D. O.; Silva Júnior, Wilson Araújo da
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: NEOPLASIAS OVARIANAS, MULHERES, MORTE
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ABNT
MUYS, B. R. et al. MiR-450a and miR-450b-5p negatively impact the tumorigenic potential of ovarian epithelial cancer cells. 2017, Anais.. Orlando: ASHG, 2017. . Acesso em: 03 jun. 2024.
APA
Muys, B. R., Sousa, J. F., Araújo, L. F., Turaça, F., Rodrigues, I. S., Vidal, D. O., & Silva Júnior, W. A. da. (2017). MiR-450a and miR-450b-5p negatively impact the tumorigenic potential of ovarian epithelial cancer cells. In Abstracts. Orlando: ASHG.
NLM
Muys BR, Sousa JF, Araújo LF, Turaça F, Rodrigues IS, Vidal DO, Silva Júnior WA da. MiR-450a and miR-450b-5p negatively impact the tumorigenic potential of ovarian epithelial cancer cells. Abstracts. 2017 ;[citado 2024 jun. 03 ]
Vancouver
Muys BR, Sousa JF, Araújo LF, Turaça F, Rodrigues IS, Vidal DO, Silva Júnior WA da. MiR-450a and miR-450b-5p negatively impact the tumorigenic potential of ovarian epithelial cancer cells. Abstracts. 2017 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions (2015)
Markello, T.; Marchegiani, S.; Davis, T.; Tessadori, F.; van Haaften, G.; Brancati, F.; Pusey, B.; Wolfe, L.; Tifft, C.; Ferraz, Victor Evangelista de Faria; Roche, N.; Ramos, F.; Malicdan, M.; Boerkoel, C.; Gahl, W. A.; Vries, B. de; van Haelst, M.; Zenker, M.
Source: Poster Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: MACROSTOMIA, DOENÇAS GENÉTICAS
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ABNT
MARKELLO, T. et al. TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 03 jun. 2024.
APA
Markello, T., Marchegiani, S., Davis, T., Tessadori, F., van Haaften, G., Brancati, F., et al. (2015). TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions. In Poster Abstracts. Baltimore: ASHG.
NLM
Markello T, Marchegiani S, Davis T, Tessadori F, van Haaften G, Brancati F, Pusey B, Wolfe L, Tifft C, Ferraz VE de F, Roche N, Ramos F, Malicdan M, Boerkoel C, Gahl WA, Vries B de, van Haelst M, Zenker M. TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Vancouver
Markello T, Marchegiani S, Davis T, Tessadori F, van Haaften G, Brancati F, Pusey B, Wolfe L, Tifft C, Ferraz VE de F, Roche N, Ramos F, Malicdan M, Boerkoel C, Gahl WA, Vries B de, van Haelst M, Zenker M. TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Application of fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) for detecting PTEN loss in diagnostic prostate cancer needle biopsies (2015)
Squire, Jeremy Andrew; Picanco-Albuquerque, C. G.; Morais, C. L.; Carvalho, F. L. F.; Peskoe, S. B.; Hicks, J. L.; Ludkovski, O.; Fedor, H.; Humphreys, E.; Han, M.; Platz, E. A.; Marzo, A. M. de; Berman, D. M.; Lotan, D. L.
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: NEOPLASIAS PROSTÁTICAS (DIAGNÓSTICO), HIBRIDIZAÇÃO
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ABNT
SQUIRE, Jeremy Andrew et al. Application of fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) for detecting PTEN loss in diagnostic prostate cancer needle biopsies. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 03 jun. 2024.
APA
Squire, J. A., Picanco-Albuquerque, C. G., Morais, C. L., Carvalho, F. L. F., Peskoe, S. B., Hicks, J. L., et al. (2015). Application of fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) for detecting PTEN loss in diagnostic prostate cancer needle biopsies. In Abstracts. Baltimore: ASHG.
NLM
Squire JA, Picanco-Albuquerque CG, Morais CL, Carvalho FLF, Peskoe SB, Hicks JL, Ludkovski O, Fedor H, Humphreys E, Han M, Platz EA, Marzo AM de, Berman DM, Lotan DL. Application of fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) for detecting PTEN loss in diagnostic prostate cancer needle biopsies. Abstracts. 2015 ;[citado 2024 jun. 03 ]
Vancouver
Squire JA, Picanco-Albuquerque CG, Morais CL, Carvalho FLF, Peskoe SB, Hicks JL, Ludkovski O, Fedor H, Humphreys E, Han M, Platz EA, Marzo AM de, Berman DM, Lotan DL. Application of fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) for detecting PTEN loss in diagnostic prostate cancer needle biopsies. Abstracts. 2015 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Admixture and ancestry patterns of three Brazilian quilombo remnants communities (2015)
Mendes Júnior, Celso Teixeira; Salvanha, D. M.; Vêncio, Ricardo Zorzetto Nicoliello; Garrido, Leandro Maza; Krieger, Henrique; Castelli, E. C.; Simões, Aguinaldo Luiz; Andrade, E. S
Source: Poster Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FFCLRP, ICB, FMRP
Subjects: QUILOMBOS, ASCENDENTE, GRUPOS ÉTNICOS
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ABNT
MENDES JÚNIOR, Celso Teixeira et al. Admixture and ancestry patterns of three Brazilian quilombo remnants communities. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 03 jun. 2024.
APA
Mendes Júnior, C. T., Salvanha, D. M., Vêncio, R. Z. N., Garrido, L. M., Krieger, H., Castelli, E. C., et al. (2015). Admixture and ancestry patterns of three Brazilian quilombo remnants communities. In Poster Abstracts. Baltimore: ASHG.
NLM
Mendes Júnior CT, Salvanha DM, Vêncio RZN, Garrido LM, Krieger H, Castelli EC, Simões AL, Andrade ES. Admixture and ancestry patterns of three Brazilian quilombo remnants communities. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Vancouver
Mendes Júnior CT, Salvanha DM, Vêncio RZN, Garrido LM, Krieger H, Castelli EC, Simões AL, Andrade ES. Admixture and ancestry patterns of three Brazilian quilombo remnants communities. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals (2015)
Carvalho, S. C. S.; Grangeiro, C. H. P.; Albuquerque, C. G. P.; Anjos, T. O.; Plaça, J. R.; Araújo, L. F.; Muys, B. R.; Souza, E. M.; Molfetta, Greice Andreotti de; Silva Júnior, Wilson Araújo da; Ferraz, Victor Evangelista de Faria
Source: Poster Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: SURDEZ, GENÉTICA MÉDICA, DIAGNÓSTICO
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ABNT
CARVALHO, S. C. S. et al. Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 03 jun. 2024.
APA
Carvalho, S. C. S., Grangeiro, C. H. P., Albuquerque, C. G. P., Anjos, T. O., Plaça, J. R., Araújo, L. F., et al. (2015). Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals. In Poster Abstracts. Baltimore: ASHG.
NLM
Carvalho SCS, Grangeiro CHP, Albuquerque CGP, Anjos TO, Plaça JR, Araújo LF, Muys BR, Souza EM, Molfetta GA de, Silva Júnior WA da, Ferraz VE de F. Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Vancouver
Carvalho SCS, Grangeiro CHP, Albuquerque CGP, Anjos TO, Plaça JR, Araújo LF, Muys BR, Souza EM, Molfetta GA de, Silva Júnior WA da, Ferraz VE de F. Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome (2015)
Souza, E. M. S. M. M.; Peronni, K. C.; Plaça, J. R.; Molfetta, Greice Andreotti de; Carvalho, S. C. S.; Marques, A. A.; Araújo, L. F.; Silva Júnior, Wilson Araújo da; Ferraz, Victor Evangelista de Faria
Source: Poster Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: MACROSTOMIA, DOENÇAS GENÉTICAS
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ABNT
SOUZA, E. M. S. M. M. et al. Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 03 jun. 2024.
APA
Souza, E. M. S. M. M., Peronni, K. C., Plaça, J. R., Molfetta, G. A. de, Carvalho, S. C. S., Marques, A. A., et al. (2015). Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome. In Poster Abstracts. Baltimore: ASHG.
NLM
Souza EMSMM, Peronni KC, Plaça JR, Molfetta GA de, Carvalho SCS, Marques AA, Araújo LF, Silva Júnior WA da, Ferraz VE de F. Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Vancouver
Souza EMSMM, Peronni KC, Plaça JR, Molfetta GA de, Carvalho SCS, Marques AA, Araújo LF, Silva Júnior WA da, Ferraz VE de F. Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services (2015)
Molfetta, Greice Andreotti de; Marques, A.; Furtado, C.; Ramos, Ester Silveira; Silva Júnior, Wilson Araújo da
Source: Poster Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: SÍNDROME X, ACONSELHAMENTO GENÉTICO
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ABNT
MOLFETTA, Greice Andreotti de et al. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 03 jun. 2024.
APA
Molfetta, G. A. de, Marques, A., Furtado, C., Ramos, E. S., & Silva Júnior, W. A. da. (2015). Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. In Poster Abstracts. Baltimore: ASHG.
NLM
Molfetta GA de, Marques A, Furtado C, Ramos ES, Silva Júnior WA da. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Vancouver
Molfetta GA de, Marques A, Furtado C, Ramos ES, Silva Júnior WA da. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Genotype-phenotype correlation of an 8p complex rearrangement (2015)
Martelli, Lúcia Regina; Grangeiro, Carlos Henrique Paiva; Gomes, A. G.; Joaquim, T. M; Laureano, L. A. F.; Grzesiuk, J. D.; Gennaro, F. G. O.; Huber, Jair; Squire, Jeremy Andrew
Source: Poster Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: GENÓTIPOS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTELLI, Lúcia Regina et al. Genotype-phenotype correlation of an 8p complex rearrangement. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 03 jun. 2024.
APA
Martelli, L. R., Grangeiro, C. H. P., Gomes, A. G., Joaquim, T. M., Laureano, L. A. F., Grzesiuk, J. D., et al. (2015). Genotype-phenotype correlation of an 8p complex rearrangement. In Poster Abstracts. Baltimore: ASHG.
NLM
Martelli LR, Grangeiro CHP, Gomes AG, Joaquim TM, Laureano LAF, Grzesiuk JD, Gennaro FGO, Huber J, Squire JA. Genotype-phenotype correlation of an 8p complex rearrangement. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Vancouver
Martelli LR, Grangeiro CHP, Gomes AG, Joaquim TM, Laureano LAF, Grzesiuk JD, Gennaro FGO, Huber J, Squire JA. Genotype-phenotype correlation of an 8p complex rearrangement. Poster Abstracts. 2015 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Hox pattern expression and non coding transcripts in the HOX locus are associated with adult medulloblastoma subtype (2014)
Fontes, Aparecida Maria; Abraham, Kuruvilla Joseph ; Pinheiro, D. G.; Covas, Dimas Tadeu; Veiga, J. B.; Tirapelli, Daniela Pretti da Cunha; Ramalho, Fernando Silva; Cardoso, A. A.; Gerson, S. L.; Carlotti Júnior, Carlos Gilberto
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: GENÉTICA, GENES, MEDULOBLASTOMA (ANÁLISE GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FONTES, Aparecida Maria et al. Hox pattern expression and non coding transcripts in the HOX locus are associated with adult medulloblastoma subtype. 2014, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2014. . Acesso em: 03 jun. 2024.
APA
Fontes, A. M., Abraham, K. J., Pinheiro, D. G., Covas, D. T., Veiga, J. B., Tirapelli, D. P. da C., et al. (2014). Hox pattern expression and non coding transcripts in the HOX locus are associated with adult medulloblastoma subtype. In Abstracts. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Fontes AM, Abraham KJ, Pinheiro DG, Covas DT, Veiga JB, Tirapelli DP da C, Ramalho FS, Cardoso AA, Gerson SL, Carlotti Júnior CG. Hox pattern expression and non coding transcripts in the HOX locus are associated with adult medulloblastoma subtype. Abstracts. 2014 ;[citado 2024 jun. 03 ]
Vancouver
Fontes AM, Abraham KJ, Pinheiro DG, Covas DT, Veiga JB, Tirapelli DP da C, Ramalho FS, Cardoso AA, Gerson SL, Carlotti Júnior CG. Hox pattern expression and non coding transcripts in the HOX locus are associated with adult medulloblastoma subtype. Abstracts. 2014 ;[citado 2024 jun. 03 ]
Trabalho de evento
Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family (2014)
Mingroni Netto, Regina Celia ; Dantas, V. G. L.; Freitas, E.L.; Moraes, A. M. S. M.; Braga, M. C. C.; Ramos, S. B.; Rosenberg, Carla ; Della-Rosa, V.A.
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, MAPEAMENTO GENÉTICO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia et al. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family. 2014, Anais.. Boston: Instituto de Biociências, Universidade de São Paulo, 2014. Disponível em: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm. Acesso em: 03 jun. 2024.
APA
Mingroni Netto, R. C., Dantas, V. G. L., Freitas, E. L., Moraes, A. M. S. M., Braga, M. C. C., Ramos, S. B., et al. (2014). Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family. In Abstracts. Boston: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
NLM
Mingroni Netto RC, Dantas VGL, Freitas EL, Moraes AMSM, Braga MCC, Ramos SB, Rosenberg C, Della-Rosa VA. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family [Internet]. Abstracts. 2014 ;[citado 2024 jun. 03 ] Available from: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
Vancouver
Mingroni Netto RC, Dantas VGL, Freitas EL, Moraes AMSM, Braga MCC, Ramos SB, Rosenberg C, Della-Rosa VA. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family [Internet]. Abstracts. 2014 ;[citado 2024 jun. 03 ] Available from: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
Trabalho de evento-resumo
Participation of individual genes, signaling pathways and biological processes related to inflammation in gestational diabetes mellitus (2013)
Cezar, N. B.; Evangelista, A. F.; Xavier, D. J.; Assis, A. F.; Ams, T. C.; Foss-Freitas, Maria Cristina; Sakamoto-Hojo, Elza Tiemi; Donadi, Eduardo Antônio; Passos Junior, Geraldo Aleixo da Silva
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP, FORP
Subjects: GRAVIDEZ NO DIABETES, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CEZAR, N. B. et al. Participation of individual genes, signaling pathways and biological processes related to inflammation in gestational diabetes mellitus. 2013, Anais.. Boston: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2013. . Acesso em: 03 jun. 2024.
APA
Cezar, N. B., Evangelista, A. F., Xavier, D. J., Assis, A. F., Ams, T. C., Foss-Freitas, M. C., et al. (2013). Participation of individual genes, signaling pathways and biological processes related to inflammation in gestational diabetes mellitus. In Abstracts. Boston: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Cezar NB, Evangelista AF, Xavier DJ, Assis AF, Ams TC, Foss-Freitas MC, Sakamoto-Hojo ET, Donadi EA, Passos Junior GA da S. Participation of individual genes, signaling pathways and biological processes related to inflammation in gestational diabetes mellitus. Abstracts. 2013 ;[citado 2024 jun. 03 ]
Vancouver
Cezar NB, Evangelista AF, Xavier DJ, Assis AF, Ams TC, Foss-Freitas MC, Sakamoto-Hojo ET, Donadi EA, Passos Junior GA da S. Participation of individual genes, signaling pathways and biological processes related to inflammation in gestational diabetes mellitus. Abstracts. 2013 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Real-time PCR for indel markers detection in cffDNA (2013)
Santos, M. D.; Nunes, F. M. F; Simões, Aguinaldo Luiz
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Subjects: PATERNIDADE, AÇÃO DE INVESTIGAÇÃO DE PATERNIDADE, EXAME DE DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, M. D. e NUNES, F. M. F e SIMÕES, Aguinaldo Luiz. Real-time PCR for indel markers detection in cffDNA. 2013, Anais.. Boston: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2013. . Acesso em: 03 jun. 2024.
APA
Santos, M. D., Nunes, F. M. F., & Simões, A. L. (2013). Real-time PCR for indel markers detection in cffDNA. In Abstracts. Boston: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Santos MD, Nunes FMF, Simões AL. Real-time PCR for indel markers detection in cffDNA. Abstracts. 2013 ;[citado 2024 jun. 03 ]
Vancouver
Santos MD, Nunes FMF, Simões AL. Real-time PCR for indel markers detection in cffDNA. Abstracts. 2013 ;[citado 2024 jun. 03 ]
Trabalho de evento-resumo
Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population (2013)
Marano, L. A.; Simões, Aguinado Luiz; Donadi, Eduardo Antônio; Mendes Júnior, Celso Teixeira
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Subjects: POLIMORFISMO, MELANINAS, GENÉTICA DE POPULAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARANO, L. A. et al. Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population. 2013, Anais.. Boston: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2013. . Acesso em: 03 jun. 2024.
APA
Marano, L. A., Simões, A. L., Donadi, E. A., & Mendes Júnior, C. T. (2013). Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population. In Abstracts. Boston: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Marano LA, Simões AL, Donadi EA, Mendes Júnior CT. Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population. Abstracts. 2013 ;[citado 2024 jun. 03 ]
Vancouver
Marano LA, Simões AL, Donadi EA, Mendes Júnior CT. Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population. Abstracts. 2013 ;[citado 2024 jun. 03 ]

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