The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations (2014)
- Authors:
- USP affiliated authors: KREPISCHI, ANA CRISTINA VICTORINO - IB ; ROSENBERG, CARLA - IB
- Unidade: IB
- DOI: 10.1186/1750-1172-9-63
- Subjects: DOENÇAS RARAS; NEOPLASIAS; MUTAÇÃO GENÉTICA; DOENÇAS HEREDITÁRIAS; SARCOMA; DNA
- Language: Inglês
- Imprenta:
- Source:
- Título: Orphanet Journal of Rare Diseases
- ISSN: 1750-1172
- Volume/Número/Paginação/Ano: v. 9, p. 63-68, Apr. 2014
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
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: 28 dez. 2025. -
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 2025 dez. 28 ] 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 2025 dez. 28 ] Available from: https://doi.org/10.1186/1750-1172-9-63 - Cytogenetically visible inversions are formed by multiple molecular mechanisms
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Informações sobre o DOI: 10.1186/1750-1172-9-63 (Fonte: oaDOI API)
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