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: 04 out. 2024. -
APA
Fidalgo, F., Rodrigues, T., Silva, A. G., Facure, L., Nóbrega, A., Sá, B., 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 B, Duprat JP, Achatz MI, Rosenberg C, Carraro DM, Krepischi ACV. Rare germline copy number variations in hereditary cutaneous melanoma [Internet]. 2014 ;[citado 2024 out. 04 ] 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 B, Duprat JP, Achatz MI, Rosenberg C, Carraro DM, Krepischi ACV. Rare germline copy number variations in hereditary cutaneous melanoma [Internet]. 2014 ;[citado 2024 out. 04 ] 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
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- Low frequency of germline TERT and MITF mutations in Brazilian melanoma-prone patients
- An apparently balanced complex chromosome rearrangement involving seven breaks and four chromosomes in a healthy female and segregation/recombination in her affected son
- Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature
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