ReP USP - Resultado da busca

Artigo de periodico
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy (2010)
Krepischi, Ana Cristina Victorino ; Knijnenburg, Jeroen; Bertola, Debora Romeu; Kim, Chong Ae; Pearson, Peter Lees; Bijlsma, Emilia; Szuhai, Karoly; Kok, Fernando; Vianna-Morgante, Angela M ; Rosenberg, Carla
Source: Epilepsia. Unidade: IB
Subjects: EPILEPSIA, GENÉTICA, NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KREPISCHI, Ana Cristina Victorino et al. Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia, v. 51 n. 12, p. 2457-2460, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1528-1167.2010.02742.x. Acesso em: 13 nov. 2024.
APA
Krepischi, A. C. V., Knijnenburg, J., Bertola, D. R., Kim, C. A., Pearson, P. L., Bijlsma, E., et al. (2010). Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia, 51 n. 12, 2457-2460. doi:10.1111/j.1528-1167.2010.02742.x
NLM
Krepischi ACV, Knijnenburg J, Bertola DR, Kim CA, Pearson PL, Bijlsma E, Szuhai K, Kok F, Vianna-Morgante AM, Rosenberg C. Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy [Internet]. Epilepsia. 2010 ; 51 n. 12 2457-2460.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1111/j.1528-1167.2010.02742.x
Vancouver
Krepischi ACV, Knijnenburg J, Bertola DR, Kim CA, Pearson PL, Bijlsma E, Szuhai K, Kok F, Vianna-Morgante AM, Rosenberg C. Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy [Internet]. Epilepsia. 2010 ; 51 n. 12 2457-2460.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1111/j.1528-1167.2010.02742.x
Artigo de periodico
High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation (2008)
Jehee, Fernanda Sarquis; Krepischi, Ana Cristina Victorino ; Rocha, K. M.; Cavalcanti, D. P.; Kim, C. A.; Bertola, Débora Romeo; Alonso, Luís Garcia; D'Angelo, C. S.; Mazzeu, Juliana Forte; Froyen, Guy; Lugtenberg, D.; Vianna-Morgante, Angela M ; Rosenberg, Carla ; Passos-Bueno, Maria Rita
Source: Journal of Medical Genetics. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JEHEE, Fernanda Sarquis et al. High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation. Journal of Medical Genetics, v. 45, n. 7, p. 447-450, 2008Tradução . . Disponível em: https://doi.org/10.1136/jmg.2007.057042. Acesso em: 13 nov. 2024.
APA
Jehee, F. S., Krepischi, A. C. V., Rocha, K. M., Cavalcanti, D. P., Kim, C. A., Bertola, D. R., et al. (2008). High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation. Journal of Medical Genetics, 45( 7), 447-450. doi:10.1136/jmg.2007.057042
NLM
Jehee FS, Krepischi ACV, Rocha KM, Cavalcanti DP, Kim CA, Bertola DR, Alonso LG, D'Angelo CS, Mazzeu JF, Froyen G, Lugtenberg D, Vianna-Morgante AM, Rosenberg C, Passos-Bueno MR. High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation [Internet]. Journal of Medical Genetics. 2008 ; 45( 7): 447-450.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1136/jmg.2007.057042
Vancouver
Jehee FS, Krepischi ACV, Rocha KM, Cavalcanti DP, Kim CA, Bertola DR, Alonso LG, D'Angelo CS, Mazzeu JF, Froyen G, Lugtenberg D, Vianna-Morgante AM, Rosenberg C, Passos-Bueno MR. High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation [Internet]. Journal of Medical Genetics. 2008 ; 45( 7): 447-450.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1136/jmg.2007.057042
Artigo de periodico
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome (2005)
Jehee, Fernanda Sarquis; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino ; Kok, Fernando; Knijnenburg, Jeroen; Froyen, Guy; Vianna-Morgante, Angela M ; Opitz, John M.; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: CROMOSSOMO X (ANOMALIAS), MALFORMAÇÕES, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JEHEE, Fernanda Sarquis et al. An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome. American Journal of Medical Genetics, v. 139A, n. 3, p. 221-225, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30991. Acesso em: 13 nov. 2024.
APA
Jehee, F. S., Rosenberg, C., Krepischi, A. C. V., Kok, F., Knijnenburg, J., Froyen, G., et al. (2005). An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome. American Journal of Medical Genetics, 139A( 3), 221-225. doi:10.1002/ajmg.a.30991
NLM
Jehee FS, Rosenberg C, Krepischi ACV, Kok F, Knijnenburg J, Froyen G, Vianna-Morgante AM, Opitz JM, Passos-Bueno MR. An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome [Internet]. American Journal of Medical Genetics. 2005 ; 139A( 3): 221-225.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/ajmg.a.30991
Vancouver
Jehee FS, Rosenberg C, Krepischi ACV, Kok F, Knijnenburg J, Froyen G, Vianna-Morgante AM, Opitz JM, Passos-Bueno MR. An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome [Internet]. American Journal of Medical Genetics. 2005 ; 139A( 3): 221-225.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/ajmg.a.30991

USP Schools

ReP

Filtros

Authors

Subjects

Indexado em

Non normalized affiliation