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Artigo de periodico
New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements (2021)
Tavares, Vanessa Luiza Romanelli ; Guimarães-Ramos, Sofia Ligia; Zhou, Yan; Masotti, Cibele; Ezquina, Suzana; Moreira, Danielle de Paula; Buermans, Henk; Freitas, Renato S; Dunnen, Johan T Den; Twigg, Stephen R F; Passos-Bueno, Maria Rita
Fonte: Journal of Medical Genetics. Unidades: IB, BIOINFORMÁTICA
Assuntos: GENÉTICA, DOENÇAS GENÉTICAS, FENÓTIPOS, MALFORMAÇÕES, VARIAÇÃO GENÉTICA, ANORMALIDADES CRANIOFACIAIS
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ABNT
TAVARES, Vanessa Luiza Romanelli et al. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements. Journal of Medical Genetics, 2021Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2021-107825. Acesso em: 28 jun. 2024.
APA
Tavares, V. L. R., Guimarães-Ramos, S. L., Zhou, Y., Masotti, C., Ezquina, S., Moreira, D. de P., et al. (2021). New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements. Journal of Medical Genetics. doi:10.1136/jmedgenet-2021-107825
NLM
Tavares VLR, Guimarães-Ramos SL, Zhou Y, Masotti C, Ezquina S, Moreira D de P, Buermans H, Freitas RS, Dunnen JTD, Twigg SRF, Passos-Bueno MR. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 jun. 28 ] Available from: https://doi.org/10.1136/jmedgenet-2021-107825
Vancouver
Tavares VLR, Guimarães-Ramos SL, Zhou Y, Masotti C, Ezquina S, Moreira D de P, Buermans H, Freitas RS, Dunnen JTD, Twigg SRF, Passos-Bueno MR. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 jun. 28 ] Available from: https://doi.org/10.1136/jmedgenet-2021-107825
Artigo de periodico
Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer (2021)
Bandeira, Gabriel; Rocha, Katia; Lazar, Monize; Ezquina, Suzana; Yamamoto, Guilherme ; Varela, Monica; Takahashi, Vanessa; Aguena, Meire; Gollop, Thomaz; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Krepischi, Ana Cristina Victorino ; Okamoto, Oswaldo Keith
Fonte: Breast Cancer. Unidades: IB, BIOINFORMÁTICA, FM
Assuntos: NEOPLASIAS MAMÁRIAS, NEOPLASIAS OVARIANAS, DOENÇAS HEREDITÁRIAS, GENÉTICA
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ABNT
BANDEIRA, Gabriel et al. Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer. Breast Cancer, v. 28, n. 2, p. 346-354, 2021Tradução . . Disponível em: https://doi.org/10.1007/s12282-020-01165-1. Acesso em: 28 jun. 2024.
APA
Bandeira, G., Rocha, K., Lazar, M., Ezquina, S., Yamamoto, G., Varela, M., et al. (2021). Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer. Breast Cancer, 28( 2), 346-354. doi:10.1007/s12282-020-01165-1
NLM
Bandeira G, Rocha K, Lazar M, Ezquina S, Yamamoto G, Varela M, Takahashi V, Aguena M, Gollop T, Zatz M, Passos-Bueno MR, Krepischi ACV, Okamoto OK. Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer [Internet]. Breast Cancer. 2021 ; 28( 2): 346-354.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1007/s12282-020-01165-1
Vancouver
Bandeira G, Rocha K, Lazar M, Ezquina S, Yamamoto G, Varela M, Takahashi V, Aguena M, Gollop T, Zatz M, Passos-Bueno MR, Krepischi ACV, Okamoto OK. Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer [Internet]. Breast Cancer. 2021 ; 28( 2): 346-354.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1007/s12282-020-01165-1
Trabalho de evento-resumo
Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? (2018)
Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Ezquina, Suzana ; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: Abstracts. Nome do evento: ASHI Annual Meeting. Unidades: EE, IB, FM, BIOINFORMÁTICA
Assuntos: NEOPLASIAS, IDOSOS, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? 2018, Anais.. Baltimore: Escola de Enfermagem, Universidade de São Paulo, 2018. . Acesso em: 28 jun. 2024.
APA
Naslavsky, M., Yamamoto, G. L., Ezquina, S., Duarte, Y. A. de O., Passos-Bueno, M. R., & Zatz, M. (2018). Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? In Abstracts. Baltimore: Escola de Enfermagem, Universidade de São Paulo.
NLM
Naslavsky M, Yamamoto GL, Ezquina S, Duarte YA de O, Passos-Bueno MR, Zatz M. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? Abstracts. 2018 ;[citado 2024 jun. 28 ]
Vancouver
Naslavsky M, Yamamoto GL, Ezquina S, Duarte YA de O, Passos-Bueno MR, Zatz M. Cancer mutations in healthy admixed elderly: can we improve pathogenicity interpretation? Abstracts. 2018 ;[citado 2024 jun. 28 ]

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