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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Vydáno v:BMC Cancer
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2019
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6547505/
https://ncbi.nlm.nih.gov/pubmed/31159747
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-019-5756-4
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