ReP USP - Resultado da busca

Artigo de periodico
Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum (2013)
Santos, Pollyanna Almeida Costa dos; Oliveira, Silviene Fabiana de; Freitas, Erika L.; Safatle, Heloisa Pires Neto; Rosenberg, Carla ; Ferrari, Iris; Mazzeu, Juliana Forte
Source: American Journal of Medical Genetics. Part A. Unidades: IB, FMRP
Subjects: DISOSTOSE MANDIBULOFACIAL, DESENVOLVIMENTO CRANIOFACIAL, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Pollyanna Almeida Costa dos et al. Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum. American Journal of Medical Genetics. Part A, v. 164, n. 2, p. 551–553, 2013Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36231. Acesso em: 26 ago. 2024.
APA
Santos, P. A. C. dos, Oliveira, S. F. de, Freitas, E. L., Safatle, H. P. N., Rosenberg, C., Ferrari, I., & Mazzeu, J. F. (2013). Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum. American Journal of Medical Genetics. Part A, 164( 2), 551–553. doi:10.1002/ajmg.a.36231
NLM
Santos PAC dos, Oliveira SF de, Freitas EL, Safatle HPN, Rosenberg C, Ferrari I, Mazzeu JF. Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 164( 2): 551–553.[citado 2024 ago. 26 ] Available from: https://doi.org/10.1002/ajmg.a.36231
Vancouver
Santos PAC dos, Oliveira SF de, Freitas EL, Safatle HPN, Rosenberg C, Ferrari I, Mazzeu JF. Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 164( 2): 551–553.[citado 2024 ago. 26 ] Available from: https://doi.org/10.1002/ajmg.a.36231
Trabalho de evento-resumo
Complex phenotype associated with 17q21.31 microdeletion (2012)
Taylor, A. Pic; Wawruk, H. Dornelles; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino ; Safatle, H.P.N.; Ferrari, L.; Mazzeu, J.F.
Source: Posters: Cytogenetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAYLOR, A. Pic et al. Complex phenotype associated with 17q21.31 microdeletion. 2012, Anais.. São Francisco: Instituto de Biociências, Universidade de São Paulo, 2012. Disponível em: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf. Acesso em: 26 ago. 2024.
APA
Taylor, A. P., Wawruk, H. D., Rosenberg, C., Krepischi, A. C. V., Safatle, H. P. N., Ferrari, L., & Mazzeu, J. F. (2012). Complex phenotype associated with 17q21.31 microdeletion. In Posters: Cytogenetics. São Francisco: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
NLM
Taylor AP, Wawruk HD, Rosenberg C, Krepischi ACV, Safatle HPN, Ferrari L, Mazzeu JF. Complex phenotype associated with 17q21.31 microdeletion [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 ago. 26 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
Vancouver
Taylor AP, Wawruk HD, Rosenberg C, Krepischi ACV, Safatle HPN, Ferrari L, Mazzeu JF. Complex phenotype associated with 17q21.31 microdeletion [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 ago. 26 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
Trabalho de evento-resumo
Array-CGH analysis in patients with Goldenhar Syndrome (2012)
Sánchez, S.; Freitas, E.L.; Safatle, H.P.N.; Rosenberg, Carla ; Ferrari, L.; Oliveira, S.F.; Mazzeu, J.F.
Source: Posters: Cytogenetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: CROMOSSOMOS, GENÉTICA, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SÁNCHEZ, S. et al. Array-CGH analysis in patients with Goldenhar Syndrome. 2012, Anais.. São Francisco: Instituto de Biociências, Universidade de São Paulo, 2012. Disponível em: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf. Acesso em: 26 ago. 2024.
APA
Sánchez, S., Freitas, E. L., Safatle, H. P. N., Rosenberg, C., Ferrari, L., Oliveira, S. F., & Mazzeu, J. F. (2012). Array-CGH analysis in patients with Goldenhar Syndrome. In Posters: Cytogenetics. São Francisco: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
NLM
Sánchez S, Freitas EL, Safatle HPN, Rosenberg C, Ferrari L, Oliveira SF, Mazzeu JF. Array-CGH analysis in patients with Goldenhar Syndrome [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 ago. 26 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
Vancouver
Sánchez S, Freitas EL, Safatle HPN, Rosenberg C, Ferrari L, Oliveira SF, Mazzeu JF. Array-CGH analysis in patients with Goldenhar Syndrome [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 ago. 26 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
Artigo de periodico
Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome (2010)
Mazzeu, J F; Vianna-Morgante, Angela M ; Krepischi, Ana Cristina Victorino ; Oudakker, A; Rosenberg, Carla ; Szuhai, K; McGill, J; MacCrauhhan, J; Bokhoven, H van; Brunner, H G
Source: Clinical Genetics. Unidade: IB
Subjects: GENÉTICA, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAZZEU, J F et al. Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome. Clinical Genetics, v. 77 n. 4, p. 404-407, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2009.01355.x. Acesso em: 26 ago. 2024.
APA
Mazzeu, J. F., Vianna-Morgante, A. M., Krepischi, A. C. V., Oudakker, A., Rosenberg, C., Szuhai, K., et al. (2010). Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome. Clinical Genetics, 77 n. 4, 404-407. doi:10.1111/j.1399-0004.2009.01355.x
NLM
Mazzeu JF, Vianna-Morgante AM, Krepischi ACV, Oudakker A, Rosenberg C, Szuhai K, McGill J, MacCrauhhan J, Bokhoven H van, Brunner HG. Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome [Internet]. Clinical Genetics. 2010 ; 77 n. 4 404-407.[citado 2024 ago. 26 ] Available from: https://doi.org/10.1111/j.1399-0004.2009.01355.x
Vancouver
Mazzeu JF, Vianna-Morgante AM, Krepischi ACV, Oudakker A, Rosenberg C, Szuhai K, McGill J, MacCrauhhan J, Bokhoven H van, Brunner HG. Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome [Internet]. Clinical Genetics. 2010 ; 77 n. 4 404-407.[citado 2024 ago. 26 ] Available from: https://doi.org/10.1111/j.1399-0004.2009.01355.x

USP Schools

ReP

Filtros

Authors

Subjects

Indexado em

Non normalized affiliation