Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population

BACKGROUND: About 5–10% of breast/ovarian cancers are hereditary. However, for a large proportion of cases (around 50%), the genetic cause remains unknown. These cases are grouped in a separated BRCAX category. The aim of this study was to identify genomic alterations in BRCA1/BRCA2 wild-type tumor...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Oncotarget
Κύριοι συγγραφείς: Felicio, Paula Silva, Bidinotto, Lucas Tadeu, Melendez, Matias Eliseo, Grasel, Rebeca Silveira, Campacci, Natalia, Galvão, Henrique C.R., Scapulatempo-Neto, Cristovam, Dufloth, Rozany Mucha, Evangelista, Adriane Feijó, Palmero, Edenir Inêz
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Impact Journals LLC 2018
Θέματα:
Research Paper
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6007956/
https://ncbi.nlm.nih.gov/pubmed/29938003
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.25537
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