Titolo | Pubblicato in | Anno |
---|---|---|
Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer | PEERJ | 2019 |
Identification of novel BRCA1 large genomic rearrangements by a computational algorithm of amplicon-based Next-Generation Sequencing data | PEERJ | 2019 |
Coexistence of three EGFR mutations in an NSCLC patient: A brief report | THE INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS | 2018 |
Optimizing the identification of risk-relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families | CANCER MEDICINE | 2017 |
Validation of the Ion Torrent PGM sequencing for the prospective routine molecular diagnostic of colorectal cancer. | CLINICAL BIOCHEMISTRY | 2015 |
Characterization of medulloblastoma in Fanconi Anemia: a novel mutation in the BRCA2 gene and SHH molecular subgroup | BIOMARKER RESEARCH | 2015 |
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