ReP USP - Resultado da busca

Trabalho de evento-resumo
Cytogenetic study of individuals affected by mental retardation in three apaes the region of Ribeirão Preto (2010)
Abreu, L. S.; Pina Neto, João Monteiro de; Giuliani, L.; Batista, L. M.; Mazzucatto, Luiz Fernando
Source: Abstracts Book. Conference titles: Workshop do Programa de Pós-Graduação em Genética Básica, Genética Humana e Médica e Bioinformática. Unidade: FMRP
Subjects: CITOGENÉTICA, RETARDO MENTAL, CROMOSSOMOS (ESTUDO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU, L. S. et al. Cytogenetic study of individuals affected by mental retardation in three apaes the region of Ribeirão Preto. 2010, Anais.. Ribeirão Preto: FMRP/USP, 2010. . Acesso em: 19 nov. 2024.
APA
Abreu, L. S., Pina Neto, J. M. de, Giuliani, L., Batista, L. M., & Mazzucatto, L. F. (2010). Cytogenetic study of individuals affected by mental retardation in three apaes the region of Ribeirão Preto. In Abstracts Book. Ribeirão Preto: FMRP/USP.
NLM
Abreu LS, Pina Neto JM de, Giuliani L, Batista LM, Mazzucatto LF. Cytogenetic study of individuals affected by mental retardation in three apaes the region of Ribeirão Preto. Abstracts Book. 2010 ;[citado 2024 nov. 19 ]
Vancouver
Abreu LS, Pina Neto JM de, Giuliani L, Batista LM, Mazzucatto LF. Cytogenetic study of individuals affected by mental retardation in three apaes the region of Ribeirão Preto. Abstracts Book. 2010 ;[citado 2024 nov. 19 ]
Artigo de periodico
Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype (2008)
Rodríguez, Viviana Rita; Mazzucatto, Luiz Fernando; Pina Neto, João Monteiro de
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: CITOGENÉTICA, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODRÍGUEZ, Viviana Rita e MAZZUCATTO, Luiz Fernando e PINA NETO, João Monteiro de. Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype. Brazilian Journal of Medical and Biological Research, v. 41, n. 8, p. 681-683, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000800007. Acesso em: 19 nov. 2024.
APA
Rodríguez, V. R., Mazzucatto, L. F., & Pina Neto, J. M. de. (2008). Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype. Brazilian Journal of Medical and Biological Research, 41( 8), 681-683. doi:10.1590/s0100-879x2008000800007
NLM
Rodríguez VR, Mazzucatto LF, Pina Neto JM de. Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 8): 681-683.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2008000800007
Vancouver
Rodríguez VR, Mazzucatto LF, Pina Neto JM de. Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 8): 681-683.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2008000800007
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: 19 nov. 2024. , 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 2024 nov. 19 ]
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 2024 nov. 19 ]
Trabalho de evento-resumo periodico
A prospective (thre years) cytogenetical study of 114 children with congenital anomalies submitted to necropsy died between 0 to 14 years old (2001)
Pina Neto, João Monteiro de; Ortolan, D.; Fernandez, H. H. L.; Mazzucatto, Luiz Fernando; Peres, Luiz César
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Journal of Human Genetics. Unidade: FMRP
Subjects: CITOGENÉTICA, CRIANÇAS, MORTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINA NETO, João Monteiro de et al. A prospective (thre years) cytogenetical study of 114 children with congenital anomalies submitted to necropsy died between 0 to 14 years old. American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 19 nov. 2024. , 2001
APA
Pina Neto, J. M. de, Ortolan, D., Fernandez, H. H. L., Mazzucatto, L. F., & Peres, L. C. (2001). A prospective (thre years) cytogenetical study of 114 children with congenital anomalies submitted to necropsy died between 0 to 14 years old. American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Pina Neto JM de, Ortolan D, Fernandez HHL, Mazzucatto LF, Peres LC. A prospective (thre years) cytogenetical study of 114 children with congenital anomalies submitted to necropsy died between 0 to 14 years old. American Journal of Human Genetics. 2001 ; 69( 4): 323 res. 822.[citado 2024 nov. 19 ]
Vancouver
Pina Neto JM de, Ortolan D, Fernandez HHL, Mazzucatto LF, Peres LC. A prospective (thre years) cytogenetical study of 114 children with congenital anomalies submitted to necropsy died between 0 to 14 years old. American Journal of Human Genetics. 2001 ; 69( 4): 323 res. 822.[citado 2024 nov. 19 ]
Artigo de periodico
Effect of paternal age on human sperm chromosomes (2001)
Sartorelli, Elza Maria Prestes; Mazzucatto, Luiz Fernando; Pina Neto, João Monteiro de
Source: Fertility and Sterility. Unidade: FMRP
Subjects: CROMOSSOMOS SEXUAIS, ESPERMATOGÊNESE, CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SARTORELLI, Elza Maria Prestes e MAZZUCATTO, Luiz Fernando e PINA NETO, João Monteiro de. Effect of paternal age on human sperm chromosomes. Fertility and Sterility, v. 76, n. 6, p. 1119-1123, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0015-0282(01)02894-1. Acesso em: 19 nov. 2024.
APA
Sartorelli, E. M. P., Mazzucatto, L. F., & Pina Neto, J. M. de. (2001). Effect of paternal age on human sperm chromosomes. Fertility and Sterility, 76( 6), 1119-1123. doi:10.1016/s0015-0282(01)02894-1
NLM
Sartorelli EMP, Mazzucatto LF, Pina Neto JM de. Effect of paternal age on human sperm chromosomes [Internet]. Fertility and Sterility. 2001 ; 76( 6): 1119-1123.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/s0015-0282(01)02894-1
Vancouver
Sartorelli EMP, Mazzucatto LF, Pina Neto JM de. Effect of paternal age on human sperm chromosomes [Internet]. Fertility and Sterility. 2001 ; 76( 6): 1119-1123.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/s0015-0282(01)02894-1

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