Number of rare germline CNVs and TP53 mutation types (2012)
- Authors:
- Autor USP: ROSENBERG, CARLA - IB
- Unidade: IB
- DOI: 10.1186/1750-1172-7-101
- Subjects: GENÉTICA; MUTAÇÃO GENÉTICA; NEOPLASIAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Orphanet Journal of Rare Diseases
- ISSN: 1750-1172
- Volume/Número/Paginação/Ano: v. 7, art. 101, p. on-line, 2012
- 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. 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: 27 dez. 2025. -
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 2025 dez. 27 ] 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 2025 dez. 27 ] Available from: https://doi.org/10.1186/1750-1172-7-101 - Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion
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Informações sobre o DOI: 10.1186/1750-1172-7-101 (Fonte: oaDOI API)
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