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Artigo de periodico
Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil (2022)
Krepischi, Ana Cristina Victorino ; Villela, Darine; Costa, Silvia Souza da; Bertola, Débora R. ; Vianna-Morgante, Angela M ; Pearson, Peter L; Rosenberg, Carla
Source: Scientific Reports. Unidade: IB
Subjects: DOENÇAS CONGÊNITAS, CROMOSSOMOS, GENÉTICA, ACONSELHAMENTO GENÉTICO
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ABNT
KREPISCHI, Ana Cristina Victorino et al. Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil. Scientific Reports, v. 12, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-19274-6. Acesso em: 13 nov. 2024.
APA
Krepischi, A. C. V., Villela, D., Costa, S. S. da, Bertola, D. R., Vianna-Morgante, A. M., Pearson, P. L., & Rosenberg, C. (2022). Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil. Scientific Reports, 12. doi:10.1038/s41598-022-19274-6
NLM
Krepischi ACV, Villela D, Costa SS da, Bertola DR, Vianna-Morgante AM, Pearson PL, Rosenberg C. Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil [Internet]. Scientific Reports. 2022 ; 12[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/s41598-022-19274-6
Vancouver
Krepischi ACV, Villela D, Costa SS da, Bertola DR, Vianna-Morgante AM, Pearson PL, Rosenberg C. Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil [Internet]. Scientific Reports. 2022 ; 12[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/s41598-022-19274-6
Artigo de periodico
Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses (2021)
Villela, Darine ; Mazzonetto, Patricia Camacho ; Migliavacca, Michele P; Perrone, Eduardo; Guida, Gustavo; Milanezi, Maria Fernanda G; Jorge, Alexander A. L ; Ribeiro-Bicudo, Lucilene A ; Kok, Fernando ; Campagnari, Francine; Rosso-Giuliani, Liane de; Costa, Silvia Souza da; Vianna-Morgante, Angela M ; Pearson, Peter L; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: American Journal of Medical Genetics. Part A. Unidades: FM, IB
Subjects: DOENÇAS GENÉTICAS, DOENÇAS CONGÊNITAS, ANORMALIDADES CROMOSSÔMICAS, TRANSTORNO AUTÍSTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Darine et al. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. American Journal of Medical Genetics. Part A, v. 185, n. 8, p. 2335-2344, 2021Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.62237. Acesso em: 13 nov. 2024.
APA
Villela, D., Mazzonetto, P. C., Migliavacca, M. P., Perrone, E., Guida, G., Milanezi, M. F. G., et al. (2021). Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. American Journal of Medical Genetics. Part A, 185( 8), 2335-2344. doi:10.1002/ajmg.a.62237
NLM
Villela D, Mazzonetto PC, Migliavacca MP, Perrone E, Guida G, Milanezi MFG, Jorge AAL, Ribeiro-Bicudo LA, Kok F, Campagnari F, Rosso-Giuliani L de, Costa SS da, Vianna-Morgante AM, Pearson PL, Krepischi ACV, Rosenberg C. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses [Internet]. American Journal of Medical Genetics. Part A. 2021 ; 185( 8): 2335-2344.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/ajmg.a.62237
Vancouver
Villela D, Mazzonetto PC, Migliavacca MP, Perrone E, Guida G, Milanezi MFG, Jorge AAL, Ribeiro-Bicudo LA, Kok F, Campagnari F, Rosso-Giuliani L de, Costa SS da, Vianna-Morgante AM, Pearson PL, Krepischi ACV, Rosenberg C. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses [Internet]. American Journal of Medical Genetics. Part A. 2021 ; 185( 8): 2335-2344.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/ajmg.a.62237
Artigo de periodico
Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing (2021)
Villela, Darine; Barros, Juliana Sobral de; Costa, Silvia Souza da; Aguiar, Talita F. M; Campagnari, Francine; Vianna-Morgante, Angela M ; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Annals of human genetics. Unidade: IB
Subjects: GENOMAS, ANORMALIDADES CROMOSSÔMICAS, SEQUÊNCIA DO DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Darine et al. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing. Annals of human genetics, v. 85, n. Ja 2021, p. 18-26, 2021Tradução . . Disponível em: https://doi.org/10.1111/ahg.12402. Acesso em: 13 nov. 2024.
APA
Villela, D., Barros, J. S. de, Costa, S. S. da, Aguiar, T. F. M., Campagnari, F., Vianna-Morgante, A. M., et al. (2021). Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing. Annals of human genetics, 85( Ja 2021), 18-26. doi:10.1111/ahg.12402
NLM
Villela D, Barros JS de, Costa SS da, Aguiar TFM, Campagnari F, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing [Internet]. Annals of human genetics. 2021 ; 85( Ja 2021): 18-26.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1111/ahg.12402
Vancouver
Villela D, Barros JS de, Costa SS da, Aguiar TFM, Campagnari F, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing [Internet]. Annals of human genetics. 2021 ; 85( Ja 2021): 18-26.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1111/ahg.12402
Artigo de periodico
Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review (2017)
Bonaldi, Adriano; Kashiwabara, André; Araújo, Érica S. de; Pereira, Lygia da Veiga ; Paschoal, Alexandre R; Andozia, Mayra B; Villela, Darine; Rivas, Maria P; Suemoto, Claudia K; Pasqualucci, Carlos A; Grinberg, Lea T; Brentani, Helena; Maria-Engler, Silvya Stuchi ; Carraro, Dirce M; Vianna-Morgante, Angela M ; Rosenberg, Carla ; Vasques, Luciana R; Krepischi, Ana Cristina Victorino
Source: Epigenomes. Unidades: IB, FM, FCF
Subjects: METILAÇÃO DE DNA, GENOMAS, EXPRESSÃO GÊNICA, GENÉTICA MÉDICA, EPIGÊNESE GENÉTICA, EMBRIÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BONALDI, Adriano et al. Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review. Epigenomes, v. 1, n. 2, p. 1-5, 2017Tradução . . Disponível em: https://doi.org/10.3390/epigenomes1020013. Acesso em: 13 nov. 2024.
APA
Bonaldi, A., Kashiwabara, A., Araújo, É. S. de, Pereira, L. da V., Paschoal, A. R., Andozia, M. B., et al. (2017). Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review. Epigenomes, 1( 2), 1-5. doi:10.3390/epigenomes1020013
NLM
Bonaldi A, Kashiwabara A, Araújo ÉS de, Pereira L da V, Paschoal AR, Andozia MB, Villela D, Rivas MP, Suemoto CK, Pasqualucci CA, Grinberg LT, Brentani H, Maria-Engler SS, Carraro DM, Vianna-Morgante AM, Rosenberg C, Vasques LR, Krepischi ACV. Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review [Internet]. Epigenomes. 2017 ; 1( 2): 1-5.[citado 2024 nov. 13 ] Available from: https://doi.org/10.3390/epigenomes1020013
Vancouver
Bonaldi A, Kashiwabara A, Araújo ÉS de, Pereira L da V, Paschoal AR, Andozia MB, Villela D, Rivas MP, Suemoto CK, Pasqualucci CA, Grinberg LT, Brentani H, Maria-Engler SS, Carraro DM, Vianna-Morgante AM, Rosenberg C, Vasques LR, Krepischi ACV. Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review [Internet]. Epigenomes. 2017 ; 1( 2): 1-5.[citado 2024 nov. 13 ] Available from: https://doi.org/10.3390/epigenomes1020013
Artigo de periodico
Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting (2017)
Villela, Darine; Costa, Silvia Souza; Vianna-Morgante, Angela M ; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: CITOGENÉTICA MOLECULAR, SEQUÊNCIA DO DNA, GENOMAS, ANORMALIDADES CROMOSSÔMICAS, NUCLEOTÍDEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Darine et al. Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting. European Journal of Medical Genetics, v. 60, n. 12, p. 667-674, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2017.08.020. Acesso em: 13 nov. 2024.
APA
Villela, D., Costa, S. S., Vianna-Morgante, A. M., Krepischi, A. C. V., & Rosenberg, C. (2017). Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting. European Journal of Medical Genetics, 60( 12), 667-674. doi:10.1016/j.ejmg.2017.08.020
NLM
Villela D, Costa SS, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting [Internet]. European Journal of Medical Genetics. 2017 ; 60( 12): 667-674.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.ejmg.2017.08.020
Vancouver
Villela D, Costa SS, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting [Internet]. European Journal of Medical Genetics. 2017 ; 60( 12): 667-674.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.ejmg.2017.08.020

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