Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations

BACKGROUND: Hereditary cancer predisposition syndromes are responsible for approximately 5–10% of all diagnosed cancer cases. In the past, single-gene analysis of specific high risk genes was used for the determination of the genetic cause of cancer heritability in certain families. The application...

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Detalles Bibliográficos
Autores principales: Tsaousis, Georgios N., Papadopoulou, Eirini, Apessos, Angela, Agiannitopoulos, Konstantinos, Pepe, Georgia, Kampouri, Stavroula, Diamantopoulos, Nikolaos, Floros, Theofanis, Iosifidou, Rodoniki, Katopodi, Ourania, Koumarianou, Anna, Markopoulos, Christos, Papazisis, Konstantinos, Venizelos, Vasileios, Xanthakis, Ioannis, Xepapadakis, Grigorios, Banu, Eugeniu, Eniu, Dan Tudor, Negru, Serban, Stanculeanu, Dana Lucia, Ungureanu, Andrei, Ozmen, Vahit, Tansan, Sualp, Tekinel, Mehmet, Yalcin, Suayib, Nasioulas, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547505/
https://www.ncbi.nlm.nih.gov/pubmed/31159747
http://dx.doi.org/10.1186/s12885-019-5756-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547505/
https://www.ncbi.nlm.nih.gov/pubmed/31159747
http://dx.doi.org/10.1186/s12885-019-5756-4

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