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Artigo de periodico
Insights from the genetic characterization of central precocious puberty associated with multiple anomalies (2021)
Canton, Ana Pinheiro Machado ; Krepischi, Ana Cristina Victorino ; Montenegro, Luciana Ribeiro; Costa, Silvia; Rosenberg, Carla ; Steunou, Virginie; Sobrier, Marie-Laure; Santana, Lucas ; Honjo, Rachel Sayuri ; Kim, Chong Ae ; Francis de Zegher; Idkowiak, Jan; Gilligan, Lorna C; Arlt, Wiebke; Funari, Mariana Ferreira de Assis ; Jorge, Alexander Augusto de Lima ; Mendonca, Berenice Bilharinho de ; Netchine, Irène; Brito, Vinicius Nahime ; Latronico, Ana Claudia
Source: Human Reproduction. Unidades: IB, FM
Subjects: PUBERDADE PRECOCE, GENÉTICA, DOENÇAS GENÉTICAS, ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CANTON, Ana Pinheiro Machado et al. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies. Human Reproduction, v. 36, n. 2, p. 506-518, 2021Tradução . . Disponível em: https://doi.org/10.1093/humrep/deaa306. Acesso em: 04 nov. 2024.
APA
Canton, A. P. M., Krepischi, A. C. V., Montenegro, L. R., Costa, S., Rosenberg, C., Steunou, V., et al. (2021). Insights from the genetic characterization of central precocious puberty associated with multiple anomalies. Human Reproduction, 36( 2), 506-518. doi:10.1093/humrep/deaa306
NLM
Canton APM, Krepischi ACV, Montenegro LR, Costa S, Rosenberg C, Steunou V, Sobrier M-L, Santana L, Honjo RS, Kim CA, Francis de Zegher, Idkowiak J, Gilligan LC, Arlt W, Funari MF de A, Jorge AA de L, Mendonca BB de, Netchine I, Brito VN, Latronico AC. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies [Internet]. Human Reproduction. 2021 ; 36( 2): 506-518.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1093/humrep/deaa306
Vancouver
Canton APM, Krepischi ACV, Montenegro LR, Costa S, Rosenberg C, Steunou V, Sobrier M-L, Santana L, Honjo RS, Kim CA, Francis de Zegher, Idkowiak J, Gilligan LC, Arlt W, Funari MF de A, Jorge AA de L, Mendonca BB de, Netchine I, Brito VN, Latronico AC. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies [Internet]. Human Reproduction. 2021 ; 36( 2): 506-518.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1093/humrep/deaa306
Artigo de periodico
A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts (2018)
Melo, Uirá Souto; Leite, Felipe de Souza; Costa, Silvia; Rosenberg, Carla ; Zatz, Mayana
Source: Stem Cell Research. Unidade: IB
Subjects: CÉLULAS-TRONCO, GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR, MUTAÇÃO GENÉTICA, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Uirá Souto et al. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts. Stem Cell Research, v. 31, p. 52-54, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.scr.2018.07.002. Acesso em: 04 nov. 2024.
APA
Melo, U. S., Leite, F. de S., Costa, S., Rosenberg, C., & Zatz, M. (2018). A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts. Stem Cell Research, 31, 52-54. doi:10.1016/j.scr.2018.07.002
NLM
Melo US, Leite F de S, Costa S, Rosenberg C, Zatz M. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts [Internet]. Stem Cell Research. 2018 ; 31 52-54.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.scr.2018.07.002
Vancouver
Melo US, Leite F de S, Costa S, Rosenberg C, Zatz M. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts [Internet]. Stem Cell Research. 2018 ; 31 52-54.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.scr.2018.07.002
Artigo de periodico
Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies (2015)
Gamba, Bruno Faulin; Richieri-Costa, Antonio ; Costa, Silvia; Rosenberg, Carla ; Ribeiro-Bicudo, Lucilene Arilho
Source: Molecular Genetics and Genomics. Unidades: HRAC, IB
Subjects: DOENÇAS GENÉTICAS, CROMOSSOMOS HUMANOS (ANOMALIAS), MALFORMAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GAMBA, Bruno Faulin et al. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, n. Ju 2015, p. on-line, 2015Tradução . . Disponível em: https://doi.org/10.1007/s00438-015-1072-0. Acesso em: 04 nov. 2024.
APA
Gamba, B. F., Richieri-Costa, A., Costa, S., Rosenberg, C., & Ribeiro-Bicudo, L. A. (2015). Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, ( Ju 2015), on-line. doi:10.1007/s00438-015-1072-0
NLM
Gamba BF, Richieri-Costa A, Costa S, Rosenberg C, Ribeiro-Bicudo LA. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies [Internet]. Molecular Genetics and Genomics. 2015 ;( Ju 2015): on-line.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s00438-015-1072-0
Vancouver
Gamba BF, Richieri-Costa A, Costa S, Rosenberg C, Ribeiro-Bicudo LA. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies [Internet]. Molecular Genetics and Genomics. 2015 ;( Ju 2015): on-line.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s00438-015-1072-0
Trabalho de evento-resumo periodico
Does increase in genomic microarray resolution result in increased diagnostic yield? (2015)
Villela, Darine; Costa, Silvia; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Prenatal Diagnosis. Conference titles: International Conference on Prenatal Diagnosis and Therapy. Unidade: IB
Subjects: DIAGNÓSTICO PRÉ-NATAL, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Darine et al. Does increase in genomic microarray resolution result in increased diagnostic yield?. Prenatal Diagnosis. West Sussex: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/pd.4617. Acesso em: 04 nov. 2024. , 2015
APA
Villela, D., Costa, S., Krepischi, A. C. V., & Rosenberg, C. (2015). Does increase in genomic microarray resolution result in increased diagnostic yield? Prenatal Diagnosis. West Sussex: Instituto de Biociências, Universidade de São Paulo. doi:10.1002/pd.4617
NLM
Villela D, Costa S, Krepischi ACV, Rosenberg C. Does increase in genomic microarray resolution result in increased diagnostic yield? [Internet]. Prenatal Diagnosis. 2015 ; 35( 1): 27–109.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/pd.4617
Vancouver
Villela D, Costa S, Krepischi ACV, Rosenberg C. Does increase in genomic microarray resolution result in increased diagnostic yield? [Internet]. Prenatal Diagnosis. 2015 ; 35( 1): 27–109.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/pd.4617
Trabalho de evento-resumo periodico
Copy number variants in Brazilian patients with congenital hypopituirarism (2013)
Correa, Fernanda A.; Franca, Marcela M.; Canton, Ana P. M; Otto, Aline p.; Costalonga, Everlayne F.; Brito, Vinicius N.; Carvalho, Luciani R.; Costa, Silvia; Arnhold, Ivo J. P.; Jorge, Alexander Augusto de Lima; Rosenberg, Carla ; Mendonça, Berenice Bilharinho de
Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidades: FM, IB
Subjects: GLÂNDULA PITUITÁRIA, ENDOCRINOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CORREA, Fernanda A. et al. Copy number variants in Brazilian patients with congenital hypopituirarism. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 04 nov. 2024. , 2013
APA
Correa, F. A., Franca, M. M., Canton, A. P. M., Otto, A. p., Costalonga, E. F., Brito, V. N., et al. (2013). Copy number variants in Brazilian patients with congenital hypopituirarism. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Correa FA, Franca MM, Canton APM, Otto A p., Costalonga EF, Brito VN, Carvalho LR, Costa S, Arnhold IJP, Jorge AA de L, Rosenberg C, Mendonça BB de. Copy number variants in Brazilian patients with congenital hypopituirarism [Internet]. Hormone Research in Paediatrics. 2013 ; 80 161.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Correa FA, Franca MM, Canton APM, Otto A p., Costalonga EF, Brito VN, Carvalho LR, Costa S, Arnhold IJP, Jorge AA de L, Rosenberg C, Mendonça BB de. Copy number variants in Brazilian patients with congenital hypopituirarism [Internet]. Hormone Research in Paediatrics. 2013 ; 80 161.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1159/000353762

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