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Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review.
Minucci A, Scambia G, Santonocito C, Concolino P, Canu G, Mignone F, Saggese I, Guarino D, Costella A, Molinario R, De Bonis M, Ferrandina G, Petrillo M, Scaglione GL, Capoluongo E. Minucci A, et al. Among authors: canu g. Expert Rev Mol Diagn. 2015;15(10):1383-403. doi: 10.1586/14737159.2015.1081059. Epub 2015 Aug 26. Expert Rev Mol Diagn. 2015. PMID: 26306726 Review.
Phenotype heterogeneity of hyperbilirubinemia condition: the lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar syndrome type II in an Italian patient.
Minucci A, Canu G, Tellone E, Giardina B, Zuppi C, Capoluongo E. Minucci A, et al. Among authors: canu g. Blood Cells Mol Dis. 2012 Aug 15;49(2):118-9. doi: 10.1016/j.bcmd.2012.05.004. Epub 2012 May 25. Blood Cells Mol Dis. 2012. PMID: 22633750 No abstract available.
133 results