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Artigo de periodico
A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate (2013)
Izzo, Giselle; Freitas, Erika L; Krepischi, Ana Cristina Victorino ; Pearson, Peter L; Vasques, Luciana R; Passos-Bueno, Maria Rita ; Bertola, Débora R; Rosenberg, Carla
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: FISSURA LÁBIOPALATINA, MALFORMAÇÕES, DOENÇAS GENÉTICAS
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ABNT
IZZO, Giselle et al. A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate. European Journal of Medical Genetics, v. 56, n. 4, p. 222-225, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2013.01.002. Acesso em: 16 maio 2024.
APA
Izzo, G., Freitas, E. L., Krepischi, A. C. V., Pearson, P. L., Vasques, L. R., Passos-Bueno, M. R., et al. (2013). A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate. European Journal of Medical Genetics, 56( 4), 222-225. doi:10.1016/j.ejmg.2013.01.002
NLM
Izzo G, Freitas EL, Krepischi ACV, Pearson PL, Vasques LR, Passos-Bueno MR, Bertola DR, Rosenberg C. A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate [Internet]. European Journal of Medical Genetics. 2013 ; 56( 4): 222-225.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.ejmg.2013.01.002
Vancouver
Izzo G, Freitas EL, Krepischi ACV, Pearson PL, Vasques LR, Passos-Bueno MR, Bertola DR, Rosenberg C. A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate [Internet]. European Journal of Medical Genetics. 2013 ; 56( 4): 222-225.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.ejmg.2013.01.002
Trabalho de evento-resumo periodico
Genetic study by Multiplex Ligation-dependent Probe Amplification (MLPA) in synaptic genes in autism spectrum disorders (2012)
Martins, A. L. Bossolani; Nascimento, P. Pereira; Moreira, D.P.; Giunco, C.T.; Passos-Bueno, Maria Rita ; Conte, A.C. Fett
Source: Neuropsychiatrie de l'Enfance et de l'Adolescence. Conference titles: IACAPAP 2012 - World Congress. Unidade: IB
Subjects: GENÉTICA, AUTISMO
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ABNT
MARTINS, A. L. Bossolani et al. Genetic study by Multiplex Ligation-dependent Probe Amplification (MLPA) in synaptic genes in autism spectrum disorders. Neuropsychiatrie de l'Enfance et de l'Adolescence. Paris: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.neurenf.2012.04.292. Acesso em: 16 maio 2024. , 2012
APA
Martins, A. L. B., Nascimento, P. P., Moreira, D. P., Giunco, C. T., Passos-Bueno, M. R., & Conte, A. C. F. (2012). Genetic study by Multiplex Ligation-dependent Probe Amplification (MLPA) in synaptic genes in autism spectrum disorders. Neuropsychiatrie de l'Enfance et de l'Adolescence. Paris: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.neurenf.2012.04.292
NLM
Martins ALB, Nascimento PP, Moreira DP, Giunco CT, Passos-Bueno MR, Conte ACF. Genetic study by Multiplex Ligation-dependent Probe Amplification (MLPA) in synaptic genes in autism spectrum disorders [Internet]. Neuropsychiatrie de l'Enfance et de l'Adolescence. 2012 ; 60( 5): jul. S179.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.neurenf.2012.04.292
Vancouver
Martins ALB, Nascimento PP, Moreira DP, Giunco CT, Passos-Bueno MR, Conte ACF. Genetic study by Multiplex Ligation-dependent Probe Amplification (MLPA) in synaptic genes in autism spectrum disorders [Internet]. Neuropsychiatrie de l'Enfance et de l'Adolescence. 2012 ; 60( 5): jul. S179.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.neurenf.2012.04.292
Artigo de periodico
Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries (2011)
Jehee, Fernanda Sarquis; Takamori, Jean Tetsuo; Medeiros, Paula F. Vasconcelos; Pordeus, Ana Carolina B.; Latini, Flavia Roche M.; Bertola, Débora Romeo; Kim, Chong Ae; Passos-Bueno, Maria Rita
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: ANORMALIDADES CROMOSSÔMICAS, RETARDO MENTAL, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JEHEE, Fernanda Sarquis et al. Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries. European Journal of Medical Genetics, v. 54, n. 4, p. e425-e432, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2011.03.007. Acesso em: 16 maio 2024.
APA
Jehee, F. S., Takamori, J. T., Medeiros, P. F. V., Pordeus, A. C. B., Latini, F. R. M., Bertola, D. R., et al. (2011). Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries. European Journal of Medical Genetics, 54( 4), e425-e432. doi:10.1016/j.ejmg.2011.03.007
NLM
Jehee FS, Takamori JT, Medeiros PFV, Pordeus ACB, Latini FRM, Bertola DR, Kim CA, Passos-Bueno MR. Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries [Internet]. European Journal of Medical Genetics. 2011 ; 54( 4): e425-e432.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.ejmg.2011.03.007
Vancouver
Jehee FS, Takamori JT, Medeiros PFV, Pordeus ACB, Latini FRM, Bertola DR, Kim CA, Passos-Bueno MR. Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries [Internet]. European Journal of Medical Genetics. 2011 ; 54( 4): e425-e432.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.ejmg.2011.03.007
Parte de monografia/livro
New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients (1993)
Zatz, Mayana ; Vainzof, Mariz ; Passos-Bueno, Maria Rita
Source: Systeme Nerveux, Muscles et Maladies Systemiques. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e VAINZOF, Mariz e PASSOS-BUENO, Maria Rita. New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients. Systeme Nerveux, Muscles et Maladies Systemiques. Tradução . Paris: Expansion Scientifique Francaise, 1993. . . Acesso em: 16 maio 2024.
APA
Zatz, M., Vainzof, M., & Passos-Bueno, M. R. (1993). New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients. In Systeme Nerveux, Muscles et Maladies Systemiques. Paris: Expansion Scientifique Francaise.
NLM
Zatz M, Vainzof M, Passos-Bueno MR. New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients. In: Systeme Nerveux, Muscles et Maladies Systemiques. Paris: Expansion Scientifique Francaise; 1993. [citado 2024 maio 16 ]
Vancouver
Zatz M, Vainzof M, Passos-Bueno MR. New and unexpected findings following dna and dystrophin studies in brazilian dmd / bmd patients. In: Systeme Nerveux, Muscles et Maladies Systemiques. Paris: Expansion Scientifique Francaise; 1993. [citado 2024 maio 16 ]

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