ReP USP - Resultado da busca

Filtros : "Krepischi, Ana Cristina Victorino" "Orphanet Journal of Rare Diseases" Removidos: "Brigham and Women's Hospital/Harvard Med School, Boston, MA" "Brentani, Helena" "Facure, Luciana" Limpar

Filtros

Artigo de periodico
The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations (2014)
Silva, Amanda G; Krepischi, Ana Cristina Victorino ; Pearson, Peter L; Hainaut, Pierre; Rosenberg, Carla ; Achatz, Maria Isabel
Fonte: Orphanet Journal of Rare Diseases. Unidade: IB
Assuntos: DOENÇAS RARAS, NEOPLASIAS, MUTAÇÃO GENÉTICA, DOENÇAS HEREDITÁRIAS, SARCOMA, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Amanda G et al. The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations. Orphanet Journal of Rare Diseases, v. 9, p. 63-68, 2014Tradução . . Disponível em: https://doi.org/10.1186/1750-1172-9-63. Acesso em: 25 jun. 2024.
APA
Silva, A. G., Krepischi, A. C. V., Pearson, P. L., Hainaut, P., Rosenberg, C., & Achatz, M. I. (2014). The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations. Orphanet Journal of Rare Diseases, 9, 63-68. doi:10.1186/1750-1172-9-63
NLM
Silva AG, Krepischi ACV, Pearson PL, Hainaut P, Rosenberg C, Achatz MI. The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations [Internet]. Orphanet Journal of Rare Diseases. 2014 ; 9 63-68.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1186/1750-1172-9-63
Vancouver
Silva AG, Krepischi ACV, Pearson PL, Hainaut P, Rosenberg C, Achatz MI. The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations [Internet]. Orphanet Journal of Rare Diseases. 2014 ; 9 63-68.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1186/1750-1172-9-63
Artigo de periodico
Number of rare germline CNVs and TP53 mutation types (2012)
Silva, Amanda G; Achatz, Maria Isabel W; Krepischi, Ana Cristina Victorino ; Pearson, Peter Lees; Rosenberg, Carla
Fonte: Orphanet Journal of Rare Diseases. Unidade: IB
Assuntos: GENÉTICA, MUTAÇÃO GENÉTICA, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Amanda G et al. Number of rare germline CNVs and TP53 mutation types. Orphanet Journal of Rare Diseases, v. 7, p. on-line, 2012Tradução . . Disponível em: https://doi.org/10.1186/1750-1172-7-101. Acesso em: 25 jun. 2024.
APA
Silva, A. G., Achatz, M. I. W., Krepischi, A. C. V., Pearson, P. L., & Rosenberg, C. (2012). Number of rare germline CNVs and TP53 mutation types. Orphanet Journal of Rare Diseases, 7, on-line. doi:10.1186/1750-1172-7-101
NLM
Silva AG, Achatz MIW, Krepischi ACV, Pearson PL, Rosenberg C. Number of rare germline CNVs and TP53 mutation types [Internet]. Orphanet Journal of Rare Diseases. 2012 ; 7 on-line.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1186/1750-1172-7-101
Vancouver
Silva AG, Achatz MIW, Krepischi ACV, Pearson PL, Rosenberg C. Number of rare germline CNVs and TP53 mutation types [Internet]. Orphanet Journal of Rare Diseases. 2012 ; 7 on-line.[citado 2024 jun. 25 ] Available from: https://doi.org/10.1186/1750-1172-7-101

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