In recent years, the number of patients being offered BRCA1/2 testing has changed dramatically. Advances in high-throughput sequencing technology have led many diagnostic laboratories to test next-generation sequencing (NGS)-based platforms as the main technology for clinical testing. As a consequence, the proportion of novel BRCA1/2 variants detected has greatly increased. Here, we describe two novel BRCA1 large deletions detected in Italian patients affected by hereditary breast and ovarian cancer syndrome (HBOC).

Novel BRCA1 Large Genomic Rearrangements in Italian Breast/Ovarian Cancer Patients / Rizza, Roberta; Hackmann, Karl; Paris, Ida; Minucci, Angelo; De Leo, Rossella; Schrock, Evelin; Urbani, Andrea; Capoluongo, Ettore Domenico; Gelli, Gianfranco; Concolino, Paola. - In: MOLECULAR DIAGNOSIS & THERAPY. - ISSN 1177-1062. - 23:1(2019), pp. 121-126. [10.1007/s40291-018-0376-2]

Novel BRCA1 Large Genomic Rearrangements in Italian Breast/Ovarian Cancer Patients

Capoluongo;
2019

Abstract

In recent years, the number of patients being offered BRCA1/2 testing has changed dramatically. Advances in high-throughput sequencing technology have led many diagnostic laboratories to test next-generation sequencing (NGS)-based platforms as the main technology for clinical testing. As a consequence, the proportion of novel BRCA1/2 variants detected has greatly increased. Here, we describe two novel BRCA1 large deletions detected in Italian patients affected by hereditary breast and ovarian cancer syndrome (HBOC).
2019
Novel BRCA1 Large Genomic Rearrangements in Italian Breast/Ovarian Cancer Patients / Rizza, Roberta; Hackmann, Karl; Paris, Ida; Minucci, Angelo; De Leo, Rossella; Schrock, Evelin; Urbani, Andrea; Capoluongo, Ettore Domenico; Gelli, Gianfranco; Concolino, Paola. - In: MOLECULAR DIAGNOSIS & THERAPY. - ISSN 1177-1062. - 23:1(2019), pp. 121-126. [10.1007/s40291-018-0376-2]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/779462
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