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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
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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
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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
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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
Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations (2002)
Abe-Sandes, Kiyoko; Silva Júnior, Wilson Araújo da; Zago, Marco Antônio
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
ABE-SANDES, Kiyoko e SILVA JÚNIOR, Wilson Araújo da e ZAGO, Marco Antônio. Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations. European Journal of Human Genetics. [S.l.]: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2002
APA
Abe-Sandes, K., Silva Júnior, W. A. da, & Zago, M. A. (2002). Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations. European Journal of Human Genetics. Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Abe-Sandes K, Silva Júnior WA da, Zago MA. Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations. European Journal of Human Genetics. 2002 ; 10 188.[citado 2025 out. 26 ]
Vancouver
Abe-Sandes K, Silva Júnior WA da, Zago MA. Y-Chromosome biallelic polyorphisms in Afro-Brazilian populations. European Journal of Human Genetics. 2002 ; 10 188.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Primary intestinal lymphangiectasia congenital: report of one case (2002)
Assumpção, I. R.; Pfeiffer, A. Z.; Koda, Yu Kar Ling; Furuta, K. A.; Abe, Cristina Miuki Abe Jacob; Yhira, K.; Albano, Lilian Maria José; Kim, Chong Ae
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FM
Assunto: DOENÇAS LINFÁTICAS(CONGÊNITO)
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ABNT
ASSUMPÇÃO, I. R. et al. Primary intestinal lymphangiectasia congenital: report of one case. European Journal of Human Genetics. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2002
APA
Assumpção, I. R., Pfeiffer, A. Z., Koda, Y. K. L., Furuta, K. A., Abe, C. M. A. J., Yhira, K., et al. (2002). Primary intestinal lymphangiectasia congenital: report of one case. European Journal of Human Genetics. New York: Faculdade de Medicina, Universidade de São Paulo.
NLM
Assumpção IR, Pfeiffer AZ, Koda YKL, Furuta KA, Abe CMAJ, Yhira K, Albano LMJ, Kim CA. Primary intestinal lymphangiectasia congenital: report of one case. European Journal of Human Genetics. 2002 ; 10 112.[citado 2025 out. 26 ]
Vancouver
Assumpção IR, Pfeiffer AZ, Koda YKL, Furuta KA, Abe CMAJ, Yhira K, Albano LMJ, Kim CA. Primary intestinal lymphangiectasia congenital: report of one case. European Journal of Human Genetics. 2002 ; 10 112.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Further delineation of serpentine fibula-polycystic kidney syndrome (2002)
Albano, Lilian Maria Jose; Moyses, R. M.; Barba, M. F.; Paula, A. C.; Kim, Chong Ae
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FM
Subjects: RIM(PATOLOGIA), CISTOS (PATOLOGIA)
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ABNT
ALBANO, Lilian Maria Jose et al. Further delineation of serpentine fibula-polycystic kidney syndrome. European Journal of Human Genetics. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2002
APA
Albano, L. M. J., Moyses, R. M., Barba, M. F., Paula, A. C., & Kim, C. A. (2002). Further delineation of serpentine fibula-polycystic kidney syndrome. European Journal of Human Genetics. New York: Faculdade de Medicina, Universidade de São Paulo.
NLM
Albano LMJ, Moyses RM, Barba MF, Paula AC, Kim CA. Further delineation of serpentine fibula-polycystic kidney syndrome. European Journal of Human Genetics. 2002 ; 10 112.[citado 2025 out. 26 ]
Vancouver
Albano LMJ, Moyses RM, Barba MF, Paula AC, Kim CA. Further delineation of serpentine fibula-polycystic kidney syndrome. European Journal of Human Genetics. 2002 ; 10 112.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Evidences of autosomal recessive inheritance in unifocal subtype of fibromuscular dysplasia of the renal arteries (2002)
Kim, Chong Ae; Albano, Lilian M. J.; Palhares, R. B.; Mesquita, S.; Pereira, A. C.; Krieger, Jose Eduardo
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference. Unidade: FM
Subjects: ARTÉRIAS (PATOLOGIA), RIM (PATOLOGIA), DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KIM, Chong Ae et al. Evidences of autosomal recessive inheritance in unifocal subtype of fibromuscular dysplasia of the renal arteries. European Journal of Human Genetics. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2002
APA
Kim, C. A., Albano, L. M. J., Palhares, R. B., Mesquita, S., Pereira, A. C., & Krieger, J. E. (2002). Evidences of autosomal recessive inheritance in unifocal subtype of fibromuscular dysplasia of the renal arteries. European Journal of Human Genetics. New York: Faculdade de Medicina, Universidade de São Paulo.
NLM
Kim CA, Albano LMJ, Palhares RB, Mesquita S, Pereira AC, Krieger JE. Evidences of autosomal recessive inheritance in unifocal subtype of fibromuscular dysplasia of the renal arteries. European Journal of Human Genetics. 2002 ; 10 112.[citado 2025 out. 26 ]
Vancouver
Kim CA, Albano LMJ, Palhares RB, Mesquita S, Pereira AC, Krieger JE. Evidences of autosomal recessive inheritance in unifocal subtype of fibromuscular dysplasia of the renal arteries. European Journal of Human Genetics. 2002 ; 10 112.[citado 2025 out. 26 ]

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