CareLit · DOI-Nachweis · Geburtshilfe und Frauenheilkunde
Incidence of germline mutations in risk genes including BRCA1/2 in consecutive ovarian cancer (OC) patients (AGO TR-1)
DOI 10.1055/s-0036-1592705
Bibliografische Angaben
Nachweis in CareLit
Autor:innenS Kommoss, P Harter, J Hauke, F Heitz, A Reuss, F Marmé, A Heimbach, K Prieske, L Richters, A Burges, G Neidhardt, N de Gregorio, A El-Balat, F Hilpert, W Meier, M Heubner, K Kast, I Braicu, E Hahnen, R Schmutzler
ZeitschriftGeburtshilfe und Frauenheilkunde
Ausgabe10/2016
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background: Identification of families at risk for OC including recommendation for prophylactic surgery is the only effective method to reduce OC mortality. In addition, BRCA1/2 mutations are known as prognostic factor and target for treatment. Methods: Prospective counseling and testing of consecutive patients with first diagnosis or platinum sensitive relapse of invasive epithelial OC. Testing of 25 risk genes rel…
Zitieren
Zitierempfehlung
S Kommoss, P Harter, J Hauke, F Heitz, A Reuss, F Marmé, A Heimbach, K Prieske, L Richters, A Burges, G Neidhardt, N de Gregorio, A El-Balat, F Hilpert, W Meier, M Heubner, K Kast, I Braicu, E Hahnen, R Schmutzler (2016) Incidence of germline mutations in risk genes including BRCA1/2 in consecutive ovarian cancer (OC) patients (AGO TR-1). Geburtshilfe und Frauenheilkunde (10). https://doi.org/10.1055/s-0036-1592705
Mit CareLit weiterarbeiten