NGS Panels applied to Hereditary Cancer Syndromes

Cancer is among the leading causes of morbidity and mortality worldwide (Okur et al, 2017). Germline pathogenic variants for monogenic, highly penetrant cancer susceptibility genes are observed in 5%–10% of all cancers (Lu et al, 2014). Hereditary cancers due to monogenic causes are characterized by...

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Bibliographic Details
Main Author: Rodrigues, Pedro (author)
Other Authors: Theisen, Patrícia (author), Silva, Catarina (author), Vieira, Luís (author), Gonçalves, João (author)
Format: conferenceObject
Language:eng
Published: 2020
Subjects:
Cancro da Mama
Cancro Hereditário
Doenças Genéticas
Cancro Colorretal
CNV
NGS
Sequenciação de Nova Geração
Diagnóstico Molecular
Online Access:http://hdl.handle.net/10400.18/6828
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/6828

Internet

http://hdl.handle.net/10400.18/6828

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