Referências bibliográficas

Abaixo seguem as referências utilizadas para criação da ferramenta de triagem:

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D. DRAGOO, David et al. PTEN Hamartoma Tumor Syndrome/Cowden Syndrome: Genomics, Oncogenesis, and Imaging Review for Associated Lesions and Malignancy. Cancers. Houston, TX, 2021, p. 1-12. Disponível em: https://www.mdpi.com/2072-6694/13/13/3120/htm. 

 

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DOMBI, Eva et al. Activity of Selumetinib in Neurofibromatosis Type 1–Related Plexiform Neurofibromas. N Engl J Med . Bethesda, 2016, p. 2550-2560. Disponível em: https://rarediseases.org/rare-diseases/neurofibromatosis-type-1-nf1/. 

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FRIEDMAN, JM . Neurofibromatosis 1. GENEREVIEWS®. Seattle (WA), 2019, p. 1-45. Disponível em: https://www.ncbi.nlm.nih.gov/books/NBK1109/pdf/Bookshelf_NBK1109.pdf. 

 

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HUO, Yanying et al. Genetic interactions among Brca1, Brca2, Palb2, and Trp53 in mammary tumor development. NPJ Breast Cancer. [N.I.], 2021, p. 1-12. Disponível em: https://www.nature.com/articles/s41523-021-00253-5. 

 

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J MCGARRITY, Thomas; I AMOS, Christopher ; J BAKER, Maria . Peutz-Jeghers Syndrome. GENEREVIEWS®. Seattle (WA), 2016, p. 1-23. Disponível em: https://www.ncbi.nlm.nih.gov/books/NBK1266/pdf/Bookshelf_NBK1266.pdf. 

 

KAURAH, Pardeep ; G HUNTSMAN, David . Hereditary Diffuse Gastric Cancer. GENEREVIEWS®. Seattle (WA), 2018, p. 1-23. Disponível em: https://www.ncbi.nlm.nih.gov/books/NBK1139/pdf/Bookshelf_NBK1139.pdf. 

 

M. LANCASTER, Johnathan et al. Society of Gynecologic Oncology statement on risk assessment for inherited gynecologic cancer predispositions. Gynecologic Oncology. [S.l.], 2014, p. 3-7. Disponível em: https://www.gynecologiconcology-online.net/article/S0090-8258(14)01312-2/fulltext. 

 

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R BLAIR, Vanessa et al. Hereditary diffuse gastric cancer: updated clinical practice guidelines. The Lancet Oncology. [N.I.], 2020, p. 386-397. Disponível em: https://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(20)30219-9/fulltext. 

 

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