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Rare germline copy number variations in hereditary cutaneous melanoma (2014)
Fidalgo, Felipe; Rodrigues, Tatiane; Silva, Amanda Gonçalves; Facure, Luciana; Nóbrega, Amanda; Sá, Bianca Costa Soares de; Duprat, João Pereira; Achatz, Maria Isabel; Rosenberg, Carla ; Carraro, Dirce Maria; Krepischi, Ana Cristina Victorino
Nome do evento: Annual Meeting of American Association for Cancer Research. Unidade: IB
Assuntos: MELANOMA, NEOPLASIAS (GENÉTICA), MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIDALGO, Felipe et al. Rare germline copy number variations in hereditary cutaneous melanoma. 2014, Anais.. San Diego: AACR, 2014. Disponível em: http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=32d6f306-9518-4b16-a390-31bd497ca997&cKey=0cb8274c-fa8e-4165-afc3-34265a033482&mKey=6ffe1446-a164-476a-92e7-c26446874d93. Acesso em: 24 out. 2025.
APA
Fidalgo, F., Rodrigues, T., Silva, A. G., Facure, L., Nóbrega, A., Sá, B. C. S. de, et al. (2014). Rare germline copy number variations in hereditary cutaneous melanoma. In . San Diego: AACR. Recuperado de http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=32d6f306-9518-4b16-a390-31bd497ca997&cKey=0cb8274c-fa8e-4165-afc3-34265a033482&mKey=6ffe1446-a164-476a-92e7-c26446874d93
NLM
Fidalgo F, Rodrigues T, Silva AG, Facure L, Nóbrega A, Sá BCS de, Duprat JP, Achatz MI, Rosenberg C, Carraro DM, Krepischi ACV. Rare germline copy number variations in hereditary cutaneous melanoma [Internet]. 2014 ;[citado 2025 out. 24 ] Available from: http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=32d6f306-9518-4b16-a390-31bd497ca997&cKey=0cb8274c-fa8e-4165-afc3-34265a033482&mKey=6ffe1446-a164-476a-92e7-c26446874d93
Vancouver
Fidalgo F, Rodrigues T, Silva AG, Facure L, Nóbrega A, Sá BCS de, Duprat JP, Achatz MI, Rosenberg C, Carraro DM, Krepischi ACV. Rare germline copy number variations in hereditary cutaneous melanoma [Internet]. 2014 ;[citado 2025 out. 24 ] Available from: http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=32d6f306-9518-4b16-a390-31bd497ca997&cKey=0cb8274c-fa8e-4165-afc3-34265a033482&mKey=6ffe1446-a164-476a-92e7-c26446874d93
Artigo de periodico
Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast (2014)
Fidalgo, Felipe; Rodrigues, Tatiane Cristina; Pinilla, Mabel; Silva, Amanda Gonçalves; Maciel, Maria do Socorro; Rosenberg, Carla ; Andrade, Victor Piana de; Carraro, Dirce Maria; Krepischi, Ana Cristina Victorino
Fonte: Tumor Biology. Unidade: IB
Assuntos: NEOPLASIAS MAMÁRIAS, CARCINOMA DE DUCTOS INFILTRANTE, DNA, TUMOR CARCINOIDE (PROGNÓSTICO), BIOLOGIA MOLECULAR, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIDALGO, Felipe et al. Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast. Tumor Biology, v. No 2014, p. 1-14 on-line, 2014Tradução . . Disponível em: https://doi.org/10.1007/s13277-014-2786-z. Acesso em: 24 out. 2025.
APA
Fidalgo, F., Rodrigues, T. C., Pinilla, M., Silva, A. G., Maciel, M. do S., Rosenberg, C., et al. (2014). Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast. Tumor Biology, No 2014, 1-14 on-line. doi:10.1007/s13277-014-2786-z
NLM
Fidalgo F, Rodrigues TC, Pinilla M, Silva AG, Maciel M do S, Rosenberg C, Andrade VP de, Carraro DM, Krepischi ACV. Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast [Internet]. Tumor Biology. 2014 ; No 2014 1-14 on-line.[citado 2025 out. 24 ] Available from: https://doi.org/10.1007/s13277-014-2786-z
Vancouver
Fidalgo F, Rodrigues TC, Pinilla M, Silva AG, Maciel M do S, Rosenberg C, Andrade VP de, Carraro DM, Krepischi ACV. Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast [Internet]. Tumor Biology. 2014 ; No 2014 1-14 on-line.[citado 2025 out. 24 ] Available from: https://doi.org/10.1007/s13277-014-2786-z
Artigo de periodico
An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder (2014)
Cappi, Carolina; Hounie, Ana Gabriela; Mariani, Daniel B; Diniz, Juliana Belo; Silva, Aderbal R. T; Reis, Viviane N. S; Busso, Ariane F; Silva, Amanda Gonçalves; Fidalgo, Felipe; Rogatto, Silvia Regina; Miguel, Eurípedes Constantino; Krepischi, Ana Cristina Victorino ; Brentani, Helena
Fonte: PLOS ONE. Unidades: FM, IB
Assuntos: TRANSTORNO OBSESSIVO-COMPULSIVO, SEROTONINA, TRANSTORNOS MENTAIS, GENOMAS, NEUROPSIQUIATRIA, EXPRESSÃO GÊNICA, GENÉTICA (FATORES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAPPI, Carolina et al. An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder. PLOS ONE, v. 9, n. 10, 2014Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0110198. Acesso em: 24 out. 2025.
APA
Cappi, C., Hounie, A. G., Mariani, D. B., Diniz, J. B., Silva, A. R. T., Reis, V. N. S., et al. (2014). An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder. PLOS ONE, 9( 10). doi:10.1371/journal.pone.0110198
NLM
Cappi C, Hounie AG, Mariani DB, Diniz JB, Silva ART, Reis VNS, Busso AF, Silva AG, Fidalgo F, Rogatto SR, Miguel EC, Krepischi ACV, Brentani H. An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder [Internet]. PLOS ONE. 2014 ;9( 10):[citado 2025 out. 24 ] Available from: https://doi.org/10.1371/journal.pone.0110198
Vancouver
Cappi C, Hounie AG, Mariani DB, Diniz JB, Silva ART, Reis VNS, Busso AF, Silva AG, Fidalgo F, Rogatto SR, Miguel EC, Krepischi ACV, Brentani H. An inherited small microdeletion at 15q13.3 in a patient with Early- Onset Obsessive-Compulsive Disorder [Internet]. PLOS ONE. 2014 ;9( 10):[citado 2025 out. 24 ] Available from: https://doi.org/10.1371/journal.pone.0110198

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