Rare germline copy number variations in hereditary cutaneous melanoma (2014)
- Authors:
- USP affiliated authors: ROSENBERG, CARLA - IB ; KREPISCHI, ANA CRISTINA VICTORINO - IB
- Unidade: IB
- Subjects: MELANOMA; NEOPLASIAS (GENÉTICA); MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Conference titles: Annual Meeting of American Association for Cancer Research
-
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: 27 dez. 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 dez. 27 ] 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 dez. 27 ] 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 - Cytogenetically visible inversions are formed by multiple molecular mechanisms
- LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis
- Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast
- Genetic testing for idiopathic intellectual disability: use of DNA extracted from saliva for SNP Genotyping
- Does increase in genomic microarray resolution result in increased diagnostic yield?
- Insights into the somatic mutation burden of hepatoblastomas using whole exome sequencing
- Large germline copy number variations as predisposing factor in childhood neoplasms
- The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations
- Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature
- Identification of new promising germline variants in melanoma-prone patients
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
